Insecticidal anthranilamides

ABSTRACT

This invention provides compounds of Formula (1), their N-oxides and agriculturally suitable salts wherein A, B, J, R 1 , R 2 , R 3  and R 4  and n are as defined in the disclosure. Also disclosed are methods for controlling arthropods comprising contacting the arthropods or their environment with an arthropodicidally effective amount of a compound of Formula (1) and compositions containing the compounds of Formula (1).

BACKGROUND OF THE INVENTION

[0001] This invention relates to certain anthranilamides, theirN-oxides, agriculturally suitable salts and compositions, and methods oftheir use as arthropodicides in both agronomic and nonagronomicenvironments.

[0002] The control of arthropod pests is extremely important inachieving high crop efficiency. Arthropod damage to growing and storedagronomic crops can cause significant reduction in productivity andthereby result in increased costs to the consumer. The control ofarthropod pests in forestry, greenhouse crops, ornamentals, nurserycrops, stored food and fiber products, livestock, household, and publicand animal health is also important. Many products are commerciallyavailable for these purposes, but the need continues for new compoundsthat are more effective, less costly, less toxic, environmentally saferor have different modes of action.

[0003] NL 9202078 discloses N-acyl anthranilic acid derivatives ofFormula i as insecticides

[0004] wherein, inter alia,

[0005] X is a direct bond;

[0006] Y is H or C₁-C₆ alkyl;

[0007] Z is NH₂, NH(C₁-C₃ alkyl) or N(C₁-C₃ alkyl)₂; and

[0008] R¹ through R⁹ are independently H, halogen, C₁-C₆ alkyl, phenyl,hydroxy, C₁-C₆ alkoxy or C₁-C₇ acyloxy.

SUMMARY OF THE INVENTION

[0009] This invention pertains to a method for controlling arthropodscomprising contacting the arthropods or their environment with anarthropodicidally effective amount of a compound of Formula 1, itsN-oxide or agriculturally suitable salts

[0010] wherein

[0011] A and B are independently O or S;

[0012] each J is independently a phenyl or naphthyl group substitutedwith 1 to 2 R⁵ and optionally substituted with 1 to 3 R⁶;

[0013] or each J is independently a 5- or 6-membered heteroaromatic ringor an aromatic 8-, 9- or 10-membered fused heterobicyclic ring systemwherein each ring or ring system is optionally substituted with 1 to 4R⁷;

[0014] n is 1 to 4;

[0015] R¹ is H; or C₁-C₆ alkyl, C₂-C₆ alkenyl, C₂-C₆ akynyl or C₃-C₆cycloalkyl each optionally substituted with one or more substituentsselected from the group consisting of halogen, CN, NO₂, hydroxy, C₁-C₄alkoxy, C₁-C₄ alkylthio, C₁-C₄ alkylsulfinyl, C₁-C₄ alkylsulfonyl, C₂-C₄alkoxycarbonyl, C₁-C₄ alkylamino, C₂-C₈ dialkylamino and C₃-C₆cycloalkylamino; or

[0016] R¹ is C₂-C₆ alkylcarbonyl, C₂-C₆ alkoxycarbonyl, C₂-C₆alkylaminocarbonyl, C₃-C₈ dialkylaminocarbonyl or C(═A)J;

[0017] R² is H, C₁-C₆ alkyl, C₂-C₆ alkenyl, C₂-C₆ alkynyl, C₃-C₆cycloalkyl, C₁-C₄ alkoxy, C₁-C₄ alkylamino, C₂-C₈ dialkylamino, C₃-C₆cycloalkylamino, C₂-C₆ alkoxycarbonyl or C₂-C₆ alkylcarbonyl;

[0018] R³ is H; G; C₁-C₆ alkyl, C₂-C₆ alkenyl, C₂-C₆ alkynyl, C₃-C₆cycloalkyl, each optionally substituted with one or more substituentsselected from the group consisting of halogen, G, CN, NO₂, hydroxy,C₁-C₄ alkoxy, C₁-C₄ haloalkoxy, C₁-C₄ alkylthio, C₁-C₄ alkylsulfinyl,C₁-C₄ alkylsulfonyl, C₂-C₆ alkoxycarbonyl, C₂-C₆ alkylcarbonyl, C₃-C₆trialkylsilyl, or a phenyl, phenoxy or 5- or 6-membered heteroaromaticring, each ring optionally substituted with one to three substituentsindependently selected from the group consisting of C₁-C₄ alkyl, C₂-C₄alkenyl, C₂-C₄ alkynyl, C₃-C₆ cycloalkyl, C₁-C₄ haloalkyl, C₂-C₄haloalkenyl, C₂-C₄ haloalkynyl, C₃-C₆ halocycloalkyl, halogen, CN, NO₂,C₁-C₄ alkoxy, C₁-C₄ haloalkoxy, C₁-C₄ alkylthio, C₁-C₄ alkylsulfinyl,C₁-C₄ alkylsulfonyl, C₁-C₄ alkylamino, C₂-C₈ dialkylamino, C₃-C₆cycloalkylamino, C₃-C₆ (alkyl)cycloalkylamino, C₂-C₄ alkylcarbonyl,C₂-C₆ alkoxycarbonyl, C₂-C₆ alkylaminocarbonyl, C₃-C₈dialkylaminocarbonyl or C₃-C₆ trialkylsilyl; C₁-C₄ alkoxy; C₁-C₄alkylamino; C₂-C₈ dialkylamino; C₃-C₆ cycloalkylamino; C₂-C₆alkoxycarbonyl or C₂-C₆ alkylcarbonyl; or

[0019] R² and R³ can be taken together with the nitrogen to which theyare attached to form a ring containing 2 to 6 atoms of carbon andoptionally one additional atom of nitrogen, sulfur or oxygen, said ringmay be optionally substituted with 1 to 4 substituents selected from thegroup consisting of C₁-C₂ alkyl, halogen, CN, NO₂ and C₁-C₂ alkoxy;

[0020] G is a 5- or 6-membered nonaromatic carbocyclic or heterocyclicring, optionally including one or two ring members selected from thegroup consisting of C(═O), SO or S(O)₂ and optionally substituted with 1to 4 substituents selected from the group consisting of C₁-C₂ alkyl,halogen, CN, NO₂ and C₁-C₂ alkoxy;

[0021] each R⁴ is independently H, C₁-C₆ alkyl, C₂-C₆ alkenyl, C₂-C₆alkynyl, C₃-C₆ cycloalkyl, C₁-C₆ haloalkyl, C₂-C₆ haloalkenyl, C₂-C₆haloalkynyl, C₃-C₆ halocycloalkyl, halogen, CN, NO₂, hydroxy, C₁-C₄alkoxy, C₁-C₄ haloalkoxy, C₁-C₄ alkylthio, C₁-C₄ alkylsulfinyl, C₁-C₄alkylsulfonyl, C₁-C₄ haloalkylthio, C₁-C₄ haloalkylsulfinyl, C₁-C₄haloalkylsulfonyl, C₁-C₄ alkylamino, C₂-C₈ dialkylamino, C₃-C₆cycloalkylamino, or C₃-C₆ trialkylsilyl; or

[0022] each R⁴ is independently phenyl, benzyl or phenoxy, eachoptionally substituted with C₁-C₄ alkyl, C₂-C₄ alkenyl, C₂-C₄ alkynyl,C₃-C₆ cycloalkyl, C₁-C₄ haloalkyl, C₂-C₄ haloalkenyl, C₂-C₄ haloalkynyl,C₃-C₆ halocycloalkyl, halogen, CN, NO₂, C₁-C₄ alkoxy, C₁-C₄ haloalkoxy,C₁-C₄ alkylthio, C₁-C₄ alkylsulfinyl, C₁-C₄ alkylsulfonyl, C₁-C₄alkylamino, C₂-C₈ dialkylamino, C₃-C₆ cycloalkylamino, C₃-C₆(alkyl)cycloalkylamino, C₂-C₄ alkylcarbonyl, C₂-C₆ alkoxycarbonyl, C₂-C₆alkylaminocarbonyl, C₃-C₈ dialkylaminocarbonyl or C₃-C₆ trialkylsilyl;

[0023] each R⁵ is independently C₁-C₆ alkyl, C₂-C₆ alkenyl, C₂-C₆alkynyl, C₃-C₆ cycloalkyl, C₁-C₆ haloalkyl, C₂-C₆ haloalkenyl, C₂-C₆haloalkynyl, C₃-C₆ halocycloalkyl, halogen, CN, CO₂H, CONH₂, NO₂,hydroxy, C₁-C₆ alkoxy, C₁-C₆ haloalkoxy, C₁-C₆ alkylthio, C₁-C₆alkylsulfinyl, C₁-C₆ alkylsulfonyl, C₁-C₆ haloalkylthio, C₁-C₆haloalkylsulfinyl, C₁-C₆ haloalkylsulfonyl, C₁-C₆ alkylamino, C₂-C₁₂dialkylamino, or C₃-C₆ cycloalkylamino, C₂-C₆ alkylcarbonyl, C₂-C₆alkoxycarbonyl, C₂-C₆ alkylaminocarbonyl, C₃-C₈ dialkylaminocarbonyl,C₃-C₆ trialkylsilyl; or

[0024] (R⁵)₂ when attached to adjacent carbon atoms can be takentogether as —OCF₂O—, —CF₂CF₂O—, or —OCF₂CF₂O—;

[0025] each R⁶ is independently H, halogen, C₁-C₆ alkyl, C₂-C₆ alkenyl,C₂-C₆ alkynyl, C₃-C₆ cycloalkyl, C₁-C₄ alkoxy or C₂-C₄ alkoxycarbonyl;or

[0026] each R⁶ is independently a phenyl, benzyl, phenoxy, 5- or6-membered heteroaromatic ring or an aromatic 8-, 9- or 10-memberedfused heterobicyclic ring system, each ring optionally substituted withone to three substituents independently selected from the groupconsisting of C₁-C₄ alkyl, C₂-C₄ alkenyl, C₂-C₄ alkynyl, C₃-C₆cycloalkyl, C₁-C₄ haloalkyl, C₂-C₄ haloalkenyl, C₂-C₄ haloalkynyl, C₃-C₆halocycloalkyl, halogen, CN, NO₂, C₁-C₄ alkoxy, C₁-C₄ haloalkoxy, C₁-C₄alkylthio, C₁-C₄ alkylsulfinyl, C₁-C₄ alkylsulfonyl, C₁-C₄ alkylamino,C₂-C₈ dialkylamino, C₃-C₆ cycloalkylamino, C₃-C₆ (alkyl)cycloalkylamino,C₂-C₄ alkylcarbonyl, C₂-C₆ alkoxycarbonyl, C₂-C₆ alkylaminocarbonyl,C₃-C₈ dialkylaminocarbonyl or C₃-C₆ trialkylsilyl;

[0027] each R⁷ is independently H, C₁-C₆ alkyl, C₂-C₆ alkenyl, C₂-C₆alkynyl, C₃-C₆ cycloalkyl, C₁-C₆ haloalkyl, C₂-C₆ haloalkenyl, C₂-C₆haloalkynyl, C₃-C₆ halocycloalkyl, halogen, CN, CO₂H, CONH₂, NO₂,hydroxy, C₁-C₄ alkoxy, C₁-C₄ haloalkoxy, C₁-C₄ alkylthio, C₁-C₄alkylsulfinyl, C₁-C₄ alkylsulfonyl, C₁-C₄ haloalkylthio, C₁-C₄haloalkylsulfinyl, C₁-C₄ haloalkylsulfonyl, C₁-C₄ alkylamino, C₂-C₈dialkylamino, C₃-C₆ cycloalkylamino, C₂-C₆ alkylcarbonyl, C₂-C₆alkoxycarbonyl, C₂-C₆ alkylaminocarbonyl, C₃-C₈ dialkylaminocarbonyl,C₃-C₆ trialkylsilyl; or

[0028] each R⁷ is independently a phenyl, benzyl, benzoyl, phenoxy, 5-or 6-membered heteroaromatic ring or an aromatic 8-, 9- or 10-memberedfused heterobicyclic ring system, each ring optionally substituted withone to three substituents independently selected from the groupconsisting of C₁-C₄ alkyl, C₂-C₄ alkenyl, C₂-C₄ alkynyl, C₃-C₆cycloalkyl, C₁-C₄ haloalkyl, C₂-C₄ haloalkenyl, C₂-C₄ haloalkynyl, C₃-C₆halocycloalkyl, halogen, CN, NO₂, C₁-C₄ alkoxy, C₁-C₄ haloalkoxy, C₁-C₄alkylthio, C₁-C₄ alkylsulfinyl, C₁-C₄ alkylsulfonyl, C₁-C₄ alkylamino,C₂-C₈ dialkylamino, C₃-C₆ cycloalkylamino, C₃-C₆ (alkyl)cycloalkylamino,C₂-C₄ alkylcarbonyl, C₂-C₆ alkoxycarbonyl, C₂-C₆ alkylaminocarbonyl,C₃-C₈ dialkylaminocarbonyl or C₃-C₆ trialkylsilyl;

[0029] provided that

[0030] (1) when A and B are both O, R² is H or C₁-C₃ alkyl, R³ is H orC₁-C₃ alkyl and R⁴ is H, halogen, C₁-C₆ alkyl, phenyl, hydroxy or C₁-C₆alkoxy, then one R⁵ is other than halogen, C₁-C₆ alkyl, hydroxy or C₁-C₆alkoxy; or

[0031] (2) J is other than an optionally substituted 1,2,3-thiadiazole.

[0032] This invention also pertains to compounds of Formula 1, theirN-oxides and. agriculturally suitable salts

[0033] wherein

[0034] A and B are independently O or S;

[0035] each J is independently a phenyl or naphthyl group substitutedwith 1 to 2 R⁵ and optionally substituted with 1 to 3 R⁶;

[0036] or each J is independently a 5- or 6-membered heteroaromatic ringor an aromatic 8-, 9- or 10-membered fused heterobicyclic ring systemwherein each ring or ring system is optionally substituted with 1 to 4R⁷;

[0037] n is 1 to 4;

[0038] R¹ ^(_(H; or C)) ₁-C₆ alkyl, C₂-C₆ alkenyl, C₂-C₆ alkynyl orC₃-C₆ cycloalkyl each optionally substituted with one or moresubstituents selected from the group consisting of halogen, CN, NO₂,hydroxy, C₁-C₄ alkoxy, C₁-C₄ alkylthio, C₁-C₄ alkylsulfinyl, C₁-C₄alkylsulfonyl, C₂-C₄ alkoxycarbonyl, C₁-C₄ alkylamino, C₂-C₈dialkylamino and C₃-C₆ cycloalkylamino; or

[0039] R¹ is C₂-C₆ alkylcarbonyl, C₂-C₆ alkoxycarbonyl, C₂-C₆alkylaminocarbonyl, C₃-C₈ dialkylarinocarbonyl or C(═A)J;

[0040] R² is H, C₁-C₆ alkyl, C₂-C₆ alkenyl, C₂-C₆ alkynyl, C₃-C₆cycloalkyl, C₁-C₄ alkoxy, C₁-C₄ alkylamino, C₂-C₈ dialkylamino, C₃-C₆cycloalkylamino, C₂-C₆ alkoxycarbonyl or C₂-C₆ alkylcarbonyl;

[0041] R³ is H; C₁-C₆ alkyl, C₂-C₆ alkenyl, C₂-C₆ alkynyl, C₃-C₆cycloalkyl, each optionally substituted with one or more substituentsselected from the group consisting of halogen, CN, NO₂, hydroxy, C₁-C₄alkoxy, C₁-C₄ haloalkoxy, C₁-C₄ alkylthio, C₁-C₄ alkylsulfinyl, C₁-C₄alkylsulfonyl, C₂-C₆ alkoxycarbonyl, C₂-C₆ alkylcarbonyl, C₃-C₆trialkylsilyl, or a phenoxy ring optionally substituted with one tothree substituents independently selected from the group consisting ofC₁-C₄ alkyl, C₂-C₄ alkenyl, C₂-C₄ alkynyl, C₃-C₆ cycloalkyl, C₁-C₄haloalkyl, C₂-C₄ haloalkenyl, C₂-C₄ haloalkynyl, C₃-C₆ halocycloalkyl,halogen, CN, NO₂, C₁-C₄ alkoxy, C₁-C₄ haloalkoxy, C₁-C₄ alkylthio, C₁-C₄alkylsulfinyl, C₁-C₄ alkylsulfonyl, C₁-C₄ alkylamino, C₂-C₈dialkylamino, C₃-C₆ cycloalkylamino, C₃-C₆ (alkyl)cycloalkylamino, C₂-C₄alkylcarbonyl, C₂-C₆ alkoxycarbonyl, C₂-C₆ alkylaminocarbonyl, C₃-C₈dialkylaminocarbonyl or C₃-C₆ trialkylsilyl; C₁-C₄ alkoxy; C₁-C₄alkylamino; C₂-C₈ dialkylamino; C₃-C₆ cycloalkylamino; C₂-C₆alkoxycarbonyl or C₂-C₆ alkylcarbonyl; or

[0042] R² and R³ can be taken together with the nitrogen to which theyare attached to form a ring containing 2 to 6 atoms of carbon andoptionally one additional atom of nitrogen, sulfur or oxygen, said ringmay be optionally substituted with 1 to 4 substituents selected from thegroup consisting of C₁-C₂ alkyl, halogen, CN, NO₂ and C₁-C₂ alkoxy;

[0043] each R⁴ is independently H, C₁-C₆ alkyl, C₂-C₆ alkenyl, C₂-C₆alkynyl, C₃-C₆ cycloalkyl, C₁-C₆ haloalkyl, C₂-C₆ haloalkenyl, C₂-C₆haloalkynyl, C₃-C₆ halocycloalkyl, halogen, CN, NO₂, hydroxy, C₁-C₄alkoxy, C₁-C₄ haloalkoxy, C₁-C₄ alkylthio, C₁-C₄ alkylsulfinyl, C₁-C₄alkylsulfonyl, C₁-C₄ haloalkylthio, C₁-C₄ haloalkylsulfinyl, C₁-C₄haloalkylsulfonyl, C₁-C₄ alkylamino, C₂-C₈ dialkylamino, C₃-C₆cycloalkylamino, or C₃-C₆ trialkylsilyl; or

[0044] each R⁴ is independently phenyl, benzyl or phenoxy, eachoptionally substituted with C₁-C₄ alkyl, C₂-C₄ alkenyl, C₂-C₄ alkynyl,C₃-C₆ cycloalkyl, C_(1-C) ₄ haloalkyl, C₂-C₄ haloalkenyl, C₂-C₄haloalkynyl, C₃-C₆ halocycloalkyl, halogen, CN, NO₂, C₁-C₄ alkoxy, C₁-C₄haloalkoxy, C₁-C₄ alkylthio, C₁-C₄ alkylsulfinyl, C₁-C₄ alkylsulfonyl,C₁-C₄ alkylamino, C₂-C₈ dialkylamino, C₃-C₆ cycloalkylamino, C₃-C₆(alkyl)cycloalkylamino, C₂-C₄ alkylcarbonyl, C₂-C₆ alkoxycarbonyl, C₂-C₆alkylaminocarbonyl, C₃-C₈ dialkylaminocarbonyl or C₃-C₆ trialkylsilyl;

[0045] each R⁵ is independently C₁-C₆ haloalkyl, C₂-C₆ haloalkenyl,C₂-C₆ haloalkynyl, C₃-C₆ halocycloalkyl, C₁-C₄ haloalkoxy, C₁-C₄alkylthio, C₁-C₄ alkylsulfinyl, C₁-C₄ alkylsulfonyl, C₁-C₄haloalkylthio, C₁-C₄ haloalkylsulfinyl, C₁-C₄ haloalkylsulfonyl, CN,NO₂, C₁-C₄ alkoxycarbonyl, C₁-C₄ alkylamino, C₂-C₈ dialkylamino, C₃-C₆cycloalkylamino, C₂-C₆ alkylcarbonyl, C₂-C₆ alkoxycarbonyl, C₂-C₆alkylaminocarbonyl, or C₃-C₈ dialkylaminocarbonyl; or

[0046] (R⁵)₂ attached to adjacent carbon atoms can be taken together as—OCF₂O—, —CF₂CF₂O—, or —OCF₂CF₂O—;

[0047] each R⁶ is independently H, halogen, C₁-C₆ alkyl, C₂-C₆ alkenyl,C₂-C₆ alkynyl, C₃-C₆ cycloalkyl, C₁-C₄ alkoxy or C₂-C₄ alkoxycarbonyl;or

[0048] each R⁶ is independently a phenyl, benzyl, phenoxy, 5- or6-membered heteroaromatic ring or an aromatic 8-, 9- or 10-memberedfused heterobicyclic ring system, each ring optionally substituted withone to three substituents independently selected from the groupconsisting of C₁-C₄ alkyl, C₂-C₄ alkenyl, C₂-C₄ alkynyl, C₃-C₆cycloalkyl, C₁-C₄ haloalkyl, C₂-C₄ haloalkenyl, C₂-C₄ haloalkynyl C₃-C₆halocycloalkyl, halogen, CN, NO₂, C₁-C₄ haloalkoxy, C₁-C₄ alkylthio,C₁-C₄ alkylsulfinyl, C₁-C₄ alkylsulfonyl, C₁-C₄ alkylamino, C₂-C₈dialkylamino, C₃-C₆ cycloalkylamino, C₃-C₆ (alkyl)cycloalkylamino, C₂-C₄alkylcarbonyl, C₂-C₆ alkoxycarbonyl, C₂-C₆ alkylaminocarbonyl, C₃-C₈dialkylaminocarbonyl or C₃-C₆ trialkylsilyl;

[0049] each R⁷ is independently H, C₁-C₆ alkyl, C₂-C₆ alkenyl, C₂-C₆alkynyl, C₃-C₆ cycloalkyl, C₁-C₆ haloalkyl, C₂-C₆ haloalkenyl, C₂-C₆haloalkynyl, C₃-C₆ halocycloalkyl, halogen, CN, CO₂H, CONH₂, NO₂,hydroxy, C₁-C₄ alkoxy, C₁-C₄ haloalkoxy, C₁-C₄ alkylthio, C₁-C₄alkylsulfinyl, C₁-C₄ alkylsulfonyl, C₁-C₄ haloalkylthio, C₁-C₄haloalkylsulfinyl, C₁-C₄ haloalkylsulfonyl, C₁-C₄ alkylamino, C₂-C₈dialkylamino, C₃-C₆ cycloalkylamino, C₂-C₆ alkylcarbonyl, C₂-C₆alkoxycarbonyl, C₂-C₆ alkylaminocarbonyl, C₃-C₈ dialkylaminocarbonyl,C₃-C₆ trialkylsilyl; or

[0050] each R⁷ is independently a phenyl, benzyl, benzoyl, phenoxy or 5-or 6-membered heteroaromatic ring 8-, 9- or 10-membered fusedheterobicyclic ring system, each ring optionally substituted with one tothree substituents independently selected from the group consisting ofC₁-C₄ alkyl, C₂-C₄ alkenyl, C₂-C₄ alkynyl, C₃-C₆ cycloalkyl, C₁-C₄haloalkyl, C₂-C₄ haloalkenyl, C₂-C₄ haloalkyl, C₃-C₆ halocycloalkyl,halogen, CN, NO₂, C₁-C₄ alkoxy, C₁-C₄ haloalkoxy, C₁-C₄ alkylthio, C₁-C₄alkylsulfinyl, C₁-C₄ alkylsulfonyl, C₁-C₄ alkylamino, C₂-C₈dialkylamino, C₃-C₆ cycloalkylamino, C₃-C₆ (alkyl)cycloalkylamino, C₂-C₄alkylcarbonyl, C₂-C₆ alkoxycarbonyl, C₂-C₆ alkylaninocarbonyl, C₃-C₈dialkylaminocarbonyl or C₃-C₆ trialkylsilyl;

[0051] provided that

[0052] (i) at least one R⁴ and at least one R⁷ are other than H;

[0053] (ii) J is other than an optionally substituted 1,2,3-thiadiazole;

[0054] (iii) when J is an optionally substituted pyridine and R² is H,R³ is other than H or CH₃;

[0055] (iv) when J is an optionally substituted pyridine, then R⁷ cannotbe CONH₂, C₂-C₆ alkylaminocarbonyl or C₃-C₈ dialkylaminocarbonyl;

[0056] (v) when J is an optionally substituted pyrazole, tetrazole orpyrimidine, then R² and R³ cannot both be hydrogen.

[0057] This invention also pertains to arthropodicidal compositionscomprising an arthropodicidally effective amount of a compound ofFormula 1 and at least one additional component selected from the groupconsisting of surfactants, solid diluents and liquid diluents.

DETAILS OF THE INVENTION

[0058] In the above recitations, the term “alkyl”, used either alone orin compound words such as “alkylthio” or “haloalkyl” includesstraight-chain or branched alkyl, such as, methyl, ethyl, n-propyl,i-propyl, or the different butyl, pentyl or hexyl isomers. The term “1-2alkyl” indicates that one or two of the available positions for thatsubstituent may be alkyl. “Alkenyl” includes straight-chain or branchedalkenes such as 1-propenyl, 2-propenyl, and the different butenyl,pentenyl and hexenyl isomers. “Alkenyl” also includes polyenes such as1,2-propadienyl and 2,4-hexadienyl. “Alkynyl” includes straight-chain orbranched alkynes such as 1-propynyl, 2-propynyl and the differentbutynyl, pentynyl and hexynyl isomers. “Alkynyl” can also includemoieties comprised of multiple triple bonds such as 2,5-hexadiynyl.“Alkoxy” includes, for example, methoxy, ethoxy, n-propyloxy,isopropyloxy and the different butoxy, pentoxy and hexyloxy isomers.“Alkoxyalkyl” denotes alkoxy substitution on alkyl. Examples of“alkoxyalkyl” include CH₃OCH₂, CH₃OCH₂CH₂, CH₃CH₂OCH₂, CH₃CH₂CH₂CH₂OCH₂and CH₃CH₂OCH₂CH₂. “Alkylthio” includes branched or straight-chainalkylthio moieties such as methylthio, ethylthio, and the differentpropylthio, butylthio, pentylthio and hexylthio isomers. “Cycloalkyl”includes, for example, cyclopropyl, cyclobutyl, cyclopentyl andcyclohexyl.

[0059] The term “heterocyclic ring” or heterocyclic ring system” denotesrings or ring systems in which at least one ring atom is not carbon andcomprises 1 to 4 heteroatoms independently selected from the groupconsisting of nitrogen, oxygen and sulfur, provided that eachheterocyclic ring contains no more than 4 nitrogens, no more than 2oxygens and no more than 2 sulfurs. The heterocyclic ring can beattached through any available carbon or nitrogen by replacement ofhydrogen on said carbon or nitrogen. The term “aromatic ring system”denotes fully unsaturated carbocycles and heterocycles in which thepolycyclic ring system is aromatic (where aromatic indicates that theHüickel rule is satisfied for the ring system). The term “heteroaromaticring” denotes fully aromatic rings in which at least one ring atom isnot carbon and comprises 1 to 4 heteroatoms independently selected fromthe group consisting of nitrogen, oxygen and sulfur, provided that eachheterocyclic ring contains no more than 4 nitrogens, no more than 2oxygens and no more than 2 sulfurs (where aromatic indicates that theHüickel rule is satisfied). The heterocyclic ring can be attachedthrough any available carbon or nitrogen by replacement of hydrogen onsaid carbon or nitrogen. The term “aromatic heterocyclic ring system”includes fully aromatic heterocycles and heterocycles in which at leastone ring of a polycyclic ring system is aromatic (where aromaticindicates that the Hüickel rule is satisfied). The term “fusedheterobicyclic ring system” includes a ring system comprised of twofused rings in which at least one ring atom is not carbon and can bearomatic or non aromatic, as defined above.

[0060] The term “halogen”, either alone or in compound words such as“haloalkyl”, includes fluorine chlorine bromine or iodine. Further, whenused in compound words such as “haloalkyl”, said alkyl may be partiallyor fully substituted with halogen atoms which may be the same ordifferent. Examples of“haloalkyl” include F₃C, ClCH₂, CF₃CH₂ andCF₃CCl₂. The terms “haloalkenyl”, “haloalkynyl”, “haloalkoxy”, and thelike, are defined analogously to the term “haloalkyl”. Examples of“haloalkenyl” include (Cl)₂C═CHCH₂ and CF₃CH₂CH═CHCH₂. Examples of“haloalkynyl” include HC≡CCHCl, CF₃C≡C, CCl₃C≡C and FCH₂C≡CCH₂. Examplesof “haloalkoxy” include CF₃O, CCl₃CH₂O, HCF₂CH₂CH₂O and CF₃CH₂O.

[0061] The total number of carbon atoms in a substituent group isindicated by the “C_(i)-C_(j)” prefix where i and j are numbers from 1to 6. For example, C₁-C₃ alkylsulfonyl designates methylsulfonyl throughpropylsulfonyl; C₂ alkoxyalkyl designates CH₃OCH₂; C₃ alkoxyalkyldesignates, for example, CH₃CH(OCH₃), CH₃OCH₂CH₂ or CH₃CH₂OCH₂; and C₄alloxyalkyl designates the various isomers of an alkyl group substitutedwith an alkoxy group containing a total of four carbon atoms, examplesincluding CH₃CH₂CH₂OCH₂ and CH₃CH₂OCH₂CH₂. In the above recitations,when a compound of Formula 1 contains a heterocyclic ring, allsubstituents are attached to this ring through any available carbon ornitrogen by replacement of a hydrogen on said carbon or nitrogen.

[0062] When a group contains a substituent which can be hydrogen, forexample R³, then, when this substituent is taken as hydrogen, it isrecognized that this is equivalent to said group being unsubstituted.

[0063] Compounds of this invention can exist as one or morestereoisomers. The various stereoisomers include enantiomers,diastereomers, atropisomers and geometric isomers. One skilled in theart will appreciate that one stereoisomer may be more active and/or mayexhibit beneficial effects when enriched relative to the otherstercoisomer(s) or when separated from the other stereoisomer(s).Additionally, the skilled artisan knows how to separate, enrich, and/orto selectively prepare said stereoisomers. Accordingly, the compounds ofthe invention may be present as a mixture of stereoisomers, individualstereoisomers, or as an optically active form.

[0064] The present invention comprises compounds selected from Formula1, N-oxides and agriculturally suitable salts thereof. One skilled inthe art will appreciate that not all nitrogen containing heterocyclescan form N-oxides since the nitrogen requires an available lone pair foroxidation to the oxide; one skilled in the art will recognize thosenitrogen containing heterocycles which can form N-oxides. One skilled inthe art will also recognize that tertiary amines can form N-oxides.Synthetic methods for the preparation of N-oxides of heterocycles andtertiary amines are very well known by one skilled in the art includingthe oxidation of heterocycles and tertiary amines with peroxy acids suchas peracetic and m-chloroperbenzoic acid (MCPBA), hydrogen peroxide,alkyl hydroperoxides such as t-butyl hydroperoxide, sodium perborate,and dioxiranes such as dimethydioxirane. These methods for thepreparation of n-oxides have been extensively described and reviewed inthe literature, see for example: T. L. Gilchrist in ComprehensiveOrganic Synthesis, vol. 7, pp 748-750, S. V. Ley, Ed., Pergamon Press;M. Tisler and B. Stanovnik in Comprehensive Heterocyclic Chemistry, vol.3, pp 18-19, A. J. Boulton and A. McKillop, Eds., Pergamon Press; M. R.Grimmett and B. R. T. Keene in Advances in Heterocyclic Chemistry, vol.43, pp 139-151, A. R. Katritzky, Ed., Academic Press; M. Tisler and B.Stanovnik in Advances in Heterocyclic Chemistry, vol. 9, pp 285-291, A.R. Katritzky and A. J. Boulton, Eds., Academic Press; and G. W. H.Cheeseman and E. S. G. Werstiuk in Advances in Heterocyclic Chemistry,vol. 22, pp 390-392, A. R. Katritzky and A. J. Boulton, Eds., AcademicPress.

[0065] The salts of the compounds of the invention include acid-additionsalts with inorganic or organic acids such as hydrobromic, hydrochloric,nitric, phosphoric, sulfuric, acetic, butyric, fumaric, lactic, maleic,malonic, oxalic, propionic, salicylic, tartaric, 4-toluenesulfonic orvaleric acids.

[0066] Of note are certain compounds of formula II

[0067] wherein

[0068] X and Y are O;

[0069] m is 1 to 5;

[0070] n is 1 to 4;

[0071] R¹ ^(_(H; or C)) ₁-C₆ alkyl, C₂-C₆ alkenyl, C₂-C₆ alkynyl orC₃-C₆ cycloalkyl each optionally substituted with one or moresubstituents selected from the group consisting of halogen, CN, NO₂,hydroxy, C₁-C₄ alkoxy, C₁-C₄ alkylthio, C₁-C₄ alkylsulfinyl, C₁-C₄alkylsulfonyl, C₂-C₄ alkoxycarbonyl, C₁-C₄ alkylamino, C₂-C₈dialkylamino and C₃-C₆ cycloalkylamino; or

[0072] R¹ is C₂-C₆ alkylcarbonyl, C₂-C₆ alkoxycarbonyl, C₂-C₆alkylaminocarbonyl or C₃-C₈ dialkylaminocarbonyl;

[0073] R² is H, C₁-C₆ alkyl, C₂-C₆ alkenyl, C₂-C₆ alkynyl, C₃-C₆cycloalkyl, C₁-C₄ alkoxy C₁-C₄ alkylamino, C₂-C₈ dialkylamino, C₃-C₆cycloalkylamino, C₂-C₆ alkoxycarbonyl or C₂-C₆ alkylcarbonyl;

[0074] R³ is i-propyl or t-butyl; and

[0075] each R⁴ and R⁵ are independently H, C₁-C₆ alkyl, C₂-C₆ alkenyl,C₂-C₆ alkynyl, C₃-C₆ cycloalkyl, C₁-C₆ haloalkyl, C₂-C₆ haloalkenyl,C₂-C₆ haloalkynyl, C₃-C₆ halocycloalkyl, halogen, CN, CO₂H, CONH₂, NO₂,hydroxy, C₁-C₄ alkoxy, C₁-C₄ haloalkoxy, C₁-C₄ alkylthio, C₁-C₄alkylsulfinyl, C₁-C₄ alkylsulfonyl, C₁-C₄ haloalkylthio, C₁-C₄haloalkylsulfinyl, C₁-C₄ haloalkylsulfonyl, C₁-C₄ alkoxycarbonyl, C₁-C₄alkylamino, C₂-C₈ dialkylamino, C₃-C₆ cycloalkylamino, C₂-C₆alkylcarbonyl, C₂-C₆ alkoxycarbonyl, C₂-C₆ alkylaminocarbonyl, C₃-C₈dialkylaminocarbonyl, C₃-C₆ trialkylsilyl; or

[0076] each R⁴ and R⁵ are independently phenyl optionally substitutedwith C₁-C₄ alkyl, C₂-C₄ alkenyl, C₂-C₄ alkynyl, C₃-C₆ cycloalkyl, C₁-C₄haolalkyl, C₂-C₄ haloalkenyl, C₂-C₄ haloalkynyl, C₃-C₆ halocycloalkyl,halogen, CN, NO₂, C₁-C₄ alkoxy, C₁-C₄ haloalkoxy, C₁-C₄ alkylthio, C₁-C₄alkylsulfinyl, C₁-C₄ alkylsulfonyl C₁-C₄ alkoxycarbonyl, C₁-C₄alkylamino, C₂-C₈ dialkylamino, C₃-C₆ cycloalkylamino, C₃-C₆(alkyl)cycloalkylamino, C₂-C₄ alkylcarbonyl, C₂-C₆ alkoxycarbonyl, C₂-C₆alkylaminocarbonyl, C₃-C₈ dialkylaminocarbonyl or C₃-C₆ trialkylsilyl.

[0077] Also of note are methods for controlling arthropods comprisingcontacting the arthropods or their environment with an arthropodicidallyeffective amount of a compound of Formula II and insecticidalcompositions thereof.

[0078] Also of note are certain compounds of Formula III

[0079] wherein

[0080] A and B are independently O or S;

[0081] J is a phenyl group substituted with 1 to 2 R⁵ and optionallysubstituted with 1 to 3 R⁶, or a 5- or 6-membered heteroaromatic ringoptionally substituted with 1 to 4 R⁷;

[0082] n is 1 to 4;

[0083] R¹ is H; or C₁-C₆ alkyl, C₂-C₆ alkenyl, C₂-C₆ alkynyl or C₃-C₆cycloalkyl each optionally substituted with one or more substituentsselected from the group consisting of halogen, CN, NO₂, hydroxy, C₁-C₄alkoxy, C₁-C₄ alkylthio, C₁-C₄ alkylsulfinyl, C₁-C₄ alkylsulfonyl, C₂-C₄alkoxycarbonyl, C₁-C₄ alkylamino, C₂-C₈ dialkylamino and C₃-C₆cycloalkylamino; or

[0084] R¹ is C₂-C₆ alkylcarbonyl, C₂-C₆ alkoxycarbonyl, C₂-C₆alkylaminocarbonyl or C₃-C₈ dialkylaminocarbonyl;

[0085] R² is H, C₁-C₆ alkyl, C₂-C₆ alkenyl, C₂-C₆ alkynyl, C₃-C₆cycloalkyl, C₁-C₄ alkoxy, C₁-C₄ alkylamino, C₂-C₈ dialkylamino, C₃-C₆cycloalkylamino, C₂-C₆ alkoxycarbonyl or C₂-C₆ alkylcarbonyl;

[0086] R³ is H; or C₁-C₆ alkyl, C₂-C₆ alkenyl, C₂-C₆ alkynyl or C₃-C₆cycloalkyl each optionally substituted with one or more substituentsselected from the group consisting of halogen, CN, NO₂, hydroxy, C₁-C₄alkoxy, C₁-C₄ alkylthio, C₁-C₄ alkylsulfinyl and C₁-C₄ alkylsulfonyl; or

[0087] R² and R³ can be taken together with the nitrogen to which theyare attached to form a ring containing 2 to 6 atoms of carbon andoptionally one additional atom of nitrogen, sur or oxygen, said ring maybe optionally substituted with 1 to 4 substituents selected from thegroup consisting of C₁-C₂ alkyl, halogen, CN, NO₂ and C₁-C₂ alkoxy;

[0088] each R⁴ is independently H, C₁-C₆ alkyl, C₂-C₆ alkenyl, C₂-C₆alkynyl, C₃-C₆ cycloalkyl, C₁-C₆ haloalkyl, C₂-C₆ haloalkenyl, C₂-C₆haloalkynyl, C₃-C₆ halocycloalkyl, halogen, CN, CO₂H, CONH₂, NO₂,hydroxy, C₁-C₄ alkoxy, C₁-C₄ haloalkoxy, C₁-C₄ alkylthio, C₁-C₄alkylsulfinyl, C₁-C₄ alkylsulfonyl, C₁-C₄ haloalkylthio, C₁-C₄haloalkylsulfinyl, C_(l)-C₄ haloalkylsulfonyl, C₁-C₄ alkylamino, C₂-C₈dialkylamino, C₃-C₆ cycloalkylamino, C₂-C₆ alkylcarbonyl, C₂-C₆alkoxycarbonyl, C₂-C₆ alkylaminocarbonyl, C₃-C₈ dialkylaminocarbonyl,C₃-C₆ trialkylsilyl; or

[0089] each R⁴ is independently phenyl, benzyl or phenoxy, eachoptionally substituted with C₁-C₄ alkyl, C₂-C₄ alkenyl, C₂-C₄ alkynyl,C₃-C₆ cycloalkyl, C₁-C₄ haolalkyl, C₂-C₄ haloalkenyl, C₂-C₄ haloalkynyl,C₃-C₆ halocycloalkyl, halogen, CN, NO₂, C₁-C₄ alkoxy, C₁-C₄ haloalkoxy,C₁-C₄ alkylthio, C₁-C₄ alkylsulfinyl, C₁-C₄ alkylsulfonyl, C₁-C₄alkylamino, C₂-C₈ dialkylamino, C₃-C₆ cycloalkylamino, C₃-C₆(alkyl)cycloalkylamino, C₂-C₄ alkylcarbonyl, C₂-C₆ alkoxycarbonyl, C₂-C₆alkylaminocarbonyl, C₃-C₈ dialkylaminocarbonyl or C₃-C₆ trialkylsilyl;

[0090] each R⁵ is independently C₁-C₆ haloalkyl, C₂-C₆ haloalkenyl,C₂-C₆ haloalkynyl, C₃-C₆ halocycloalkyl, C₁-C₄ haloalkoxy, C₁-C₄alkylthio, C₁-C₄ alkylsulfinyl, C₁-C₄ alkylsulfonyl, C₁-C₄haloalkylthio, C₁-C₄ haloalkylsulfinyl, C₁-C₄ haloalkylsulfonyl, CN,NO₂, C₁-C₄ alkylamino, C₂-C₈ dialkylamino, C₃-C₆ cycloalkylamino, C₂-C₆alkylcarbonyl, C₂-C₆ alkoxycarbonyl, C₂-C₆ alkylaminocarbonyl, or C₃-C₈dialkylaminocarbonyl; or

[0091] (R⁵)₂ when attached to adjacent carbon atoms can be takentogether as —OCF₂O—, —CF₂CF₂O—, or —OCF₂CF₂O—;

[0092] each R⁶ is independently H, halogen, C₁-C₆ alkyl, C₂-C₆ alkenyl,C₂-C₆ alkynyl, C₃-C₆ cycloalkyl, C₁-C₄ alkoxy; or

[0093] each R⁶ is independently phenyl, benzyl or phenoxy, eachoptionally substituted with C₁-C₄ alkyl, C₂-C₄ alkenyl, C₂-C₄ alkynyl,C₃-C₆ cycloalkyl, C₁-C₄ haolalkyl, C₂-C₄ haloalkenyl, C₂-C₄ haloalkynyl,C₃-C₆ halocycloalkyl, halogen, CN, NO₂, C₁-C₄ alkoxy, C₁-C₄ haloalkoxy,C₁-C₄ alkylthio, C₁-C₄ alkylsulfinyl, C₁-C₄ alkylsulfonyl, C₁-C₄alkylamino, C₂-C₈ dialkylamino, C₃-C₆ cycloalkylamino, C₃-C₆(aklky)cycloalkylamino, C₂-C₄ alkylcarbonyl, C₂-C₆ alkoxycarbonyl, C₂-C₆alkylaminocarbonyl, C₃-C₈ dialkylaminocarbonyl or C₃-C₆ trialkylsilyl;

[0094] each R⁷ is independently H, C₁-C₆ alkyl, C₂-C₆ alkenyl, C₂-C₆alkynyl, C₃-C₆ cycloalkyl, C₁-C₆ haloalkyl, C₂-C₆ haloalkenyl, C₂-C₆haloalkynyl, C₃-C₆ halocycloalkyl, halogen, CN, CO₂H, CONH₂, NO₂,hydroxy, C₁-C₄ alkoxy, C₁-C₄ haloalkoxy, C₁-C₄ alkylthio, C₁-C₄alkylsulfinyl, C₁-C₄ alkylsulfonyl, C₁-C₄ haloalkylthio, C₁-C₄haloalkylsulfinyl, C₁-C₄ haloalkylsulfonyl, C₁-C₄ alkylamino, C₂-C₈dialkylamino, C₃-C₆ cycloalkylamino, C₂-C₆ alkylcarbonyl, C₂-C₆alkoxycarbonyl, C₂-C₆ alkylaminocarbonyl, C₃-C₈ dialkylaminocarbonyl,C₃-C₆ trialkylsilyl; or

[0095] each R⁷ is independently phenyl, benzyl or phenoxy, eachoptionally substituted with C₁-C₄ alkyl, C₂-C₄ alkenyl, C₂-C₄ alkynyl,C₃-C₆ cycloalkyl, C₁-C₄ haloalkyl, C₂-C₄ haloalkenyl, C₂-C₄ haloalkynyl,C₃-C₆ halocycloalkyl, halogen, CN, NO₂, C₁-C₄ alkoxy, C₁-C₄ haloalkoxy,C₁-C₄ alkylthio, C₁-C₄ alkylsulfinyl, C₁-C₄ alkylsulfonyl C₁-C₄alkoxycarbonyl, C₁-C₄ alkylamino, C₂-C₈ dialkylamino, C₃-C₆cycloalkylamino, C₃-C₆ (alkyl)cycloalkylamino, C₂-C₄ alkylcarbonyl,C₂-C₆ alkoxycarbonyl, C₂-C₆ alkylaminocarbonyl, C₃-C₃dialkylaminocarbonyl or C₃-C₆ trialkylsilyl.

[0096] Also of note are methods for controlling arthropods comprisingcontacting the arthropods or their environment with an arthropodicidallyeffective amount of a compound of Formula III and insecticidalcompositions thereof.

[0097] Also of note are certain compounds of Formula IV

[0098] wherein

[0099] A and B are independently O or S;

[0100] J is a phenyl group substituted with 1 to 2 R⁵ and optionallysubstituted with 1 to 3 R⁶, or a 5- or 6-membered heteroaromatic ringoptionally substituted with 1 to 4 R⁷;

[0101] n is 1 to 4;

[0102] R¹ is H; or C₁-C₆ alkyl, C₂-C₆ alkenyl, C₂-C₆ alkynyl or C₃-C₆cycloalkyl each optionally substituted with one or more substituentsselected from the group consisting of halogen, CN, NO₂, hydroxy, C₁-C₄alkoxy, C₁-C₄ alkylthio, C₁-C₄ alkylsulfinyl, C₁-C₄ alkylsulfonyl, C₂-C₄alkoxycarbonyl, C₁-C₄ alkylamino, C₂-C₈ dialkylamino and C₃-C₆cycloalkylamino; or

[0103] R¹ is C₂-C₆ alkylcarbonyl, C₂-C₆ alkoxycarbonyl, C₂-C₆alkylaminocarbonyl or C₃-C₈ dialkylaminocarbonyl;

[0104] R² is H, C₁-C₆ alkyl, C₂-C₆ alkenyl, C₂-C₆ alkynyl, C₃-C₆cycloalkyl, C₁-C₄ alkoxy, C₁-C₄ alkylamino, C₂-C₈ dialkylamino, C₃-C₆cycloalkylamino, C₂-C₆ alkoxycarbonyl or C₂-C₆ alkylcarbonyl;

[0105] R³ is H; C₁-C₆ alkyl, C₂-C₆ alkenyl, C₂-C₆ alkynyl, C₃-C₆cycloalkyl, each optionally substituted with one or more substituentsselected from the group consisting of halogen, CN, NO₂, hydroxy, C₁-C₄alkoxy, C₁-C₄ alkylthio, C₁-C₄ alkylsulfinyl and C₁-C₄ alkylsulfonyl;C₁-C₄ alkoxy; C₁-C₄alkylamino; C₂-C₈ dialkylamino; C₃-C₆cycloalkylamino; C₂-C₆ alkoxycarbonyl or C₂-C₆ alkylcarbonyl; or

[0106] R² and R³ can be taken together with the nitrogen to which theyare attached to form a ring containing 2 to 6 atoms of carbon andoptionally one additional atom of nitrogen sulfur or oxygen, said ringmay be optionally substituted with 1 to 4 substituents selected from thegroup consisting of C₁-C₂ alkyl, halogen, CN, NO₂ and C₁-C₂ alkoxy;

[0107] each R⁴ is independently H, C₁-C₆ alkyl, C₂-C₆ alkenyl, C₂-C₆alkynyl, C₃-C₆ cycloalkyl, C₁-C₆ haloalkyl, C₂-C₆ haloalkenyl, C₂-C₆haloalkynyl, C₃-C₆ halocycloalkyl, halogen, CN, CO₂H, CONH₂, NO₂,hydroxy, C₁-C₄ alkoxy, C₁-C₄ haloalkoxy, C₁-C₄ alkylthio, C₁-C₄alkylsulfinyl, C₁-C₄ alkylsulfonyl, C₁-C₄ haloalkylthio, C₁-C₄haloalkylsulfinyl, C₁-C₄ haloalkylsulfonyl, C₁-C₄ alkylamino, C₂-C₈dialkylamino, C₃-C₆ cycloalkylamino, C₂-C₆ alkylcarbonyl, C₂-C₆alkoxycarbonyl, C₂-C₆ alkylaminocarbonyl, C₃-C₈ dialkylaminocarbonyl,C₃-C₆ trialkylsilyl; or

[0108] each R⁴ is independently phenyl, benzyl or phenoxy, eachoptionally substituted with C₁-C₄ alkyl, C₂-C₄ alkenyl, C₂-C₄ alkynyl,C₃-C₆ cycloalkyl, C₁-C₄ haolalkyl, C₂-C₄ haloalkenyl, C₂-C₄ haloalkynyl,C₃-C₆ halocycloalkyl, halogen, CN, NO₂, C₁-C₄ alkoxy, C₁-C₄ haloalkoxy,C₁-C₄ alkylthio, C₁-C₄ alkylsulfinyl, C₁-C₄ alkylsulfonyl, C₁-C₄alkylamino, C₂-C₈ dialkylamino, C₃-C₆ cycloalkylamino, C₃-C₆(alkyl)cycloalkylamino, C₂-C₄ alkylcarbonyl, C₂-C₆ alkoxycarbonyl, C₂-C₆alkylaminocarbonyl, C₃-C₈ dialkylaminocarbonyl or C₃-C₆ trialkylsilyl;

[0109] each R⁵ is independently C₁-C₆ alkyl, C₂-C₆ alkenyl, C₂-C₆alkynyl, C₃-C₆ cycloalkyl, C₁-C₆ haloalkyl, C₂-C₆ haloalkenyl, C₂-C₆haloalkynyl, C₃-C₆ halocyloalkyl, halogen, CN, CO₂H, CONH₂, NO₂,hydroxy, C₁-C₄ alkoxy, C₁-C₄ haloalkoxy, C₁-C₄ alkylthio, C₁-C₄alkylsulfinyl, C₁-C₄ alkylsulfonyl, C₁-C₄ haloalkylthio, C₁-C₄haloalkylsulfinyl, C₁-C₄ haloalkylsulfonyl, C₁-C₄ alkylamino, C₂-C₈dialkylamino, C₃-C₆ cycloalkylamino, C₂-C₆ alkylcarbonyl, C₂-C₆alkoxycarbonyl, C₂-C₆ alkylaminocarbonyl, C₃-C₈ dialkylaminocarbonyl,C₃-C₆ trialkylsilyl; or

[0110] (R⁵)₂ when attached to adjacent carbon atoms can be takentogether as —OCF₂O—, —CF₂CF₂O—, or —OCF₂CF₂O—;

[0111] each R⁶ is independently H, halogen, C₁-C₆ alkyl, C₂-C₆ alkenyl,C₂-C₆ alkynyl, C₃-C₆ cycloalkyl, C₁-C₄ alkoxy; or

[0112] each R⁶ is independently a phenyl, benzyl, phenoxy or a 5- or6-membered heteroaromatic ring, each ring optionally substituted withC₁-C₄ alkyl, C₂-C₄ alkenyl, C₂-C₄ alkynyl, C₃-C₆ cycloalkyl, C₁-C₄haloalkyl, C₂-C₄ haloalkenyl, C₂-C₄ haloalkynyl, C₃-C₆ halocycloalkyl,halogen, CN, NO₂, C₁-C₄ alkoxy, C₁-C₄ haloalkoxy, C₁-C₄ alkylthio, C₁-C₄alkylsulfinyl, C₁-C₄ alkylsulfonyl, C₁-C₄ alkylamino, C₂-C₈dialkylamino, C₃-C₆ cycloalkylamino, C₃-C₆ (alkyl)cycloalkylamino, C₂-C₄alkylcarbonyl, C₂-C₆ alkoxycarbonyl, C₂-C₆ alkylaminocarbonyl C₂-C₆dialkylaminocarbonyl or C₃-C₆ trialkylsilyl;

[0113] each R⁷ is independently H, C₁-C₆ alkyl, C₂-C₆ alkenyl, C₂-C₆alkynyl, C₃-C₆ cycloalkyl, C₁-C₆ haloalkyl, C₂-C₆ haloalkenyl, C₂-C₆haloalkynyl, C₃-C₆ halocycloalkyl, halogen, CN, CO₂H, CONH₂, NO₂,hydroxy, C₁-C₄ alkoxy, C₁-C₄ haloalkoxy, C₁-C₄ alkylthio, C₁-C₄alkylsulfinyl, C₁-C₄ alkylsulfonyl, C₁-C₄ haloalkylthio, C₁-C₄haloalkylsulfinyl, C₁-C₄ haloalkylsulfonyl, C₁-C₄ alkylamino, C₂-C₈dialkylamino, C₃-C₆ cycloalkylamino, C₂-C₆ alkylcarbonyl, C₂-C₆alkoxycarbonyl, C₂-C₆ alkylaminocarbonyl, C₃-C₈ dialkylaminocarbonyl,C₃-C₆ trialkylsilyl; or

[0114] each R⁷ is independently a phenyl, benzyl, benzoyl, phenoxy or a5- or 6-membered heteroaromatic ring, each ring optionally substitutedwith C₁-C₄ alkyl, C₂-C₄ alkenyl, C₂-C₄ alkynyl, C₃-C₆ cycloalkyl, C₁-C₄haolalkyl, C₂-C₄ haloalkenyl, C₂-C₄ haloalkynyl, C₃-C₆ halocycloalkyl,halogen, CN, NO₂, C₁-C₄ alkoxy, C₁-C₄ haloalkoxy, C₁-C₄ alkylthio, C₁-C₄alkylsulfinyl, C₁-C₄ alkylsulfonyl, C₁-C₄ alkylamino, C₂-C₈dialkylamino, C₃-C₆ cycloalkylamino, C₃-C₆ (alkyl)cycloalkylamino, C₂-C₄alkylcarbonyl, C₂-C₆ alkoxycarbonyl, C₂-C₆ alkylaminocarbonyl, C₃-C₈dialkylaminocarbonyl or C₃-C₆ trialkylsilyl;

[0115] provided that when A and B are both O, R² is H or C₁-C₃ alkyl, R³is H or C₁-C₃ alkyl and R⁴ is H, halogen, C₁-C₆ alkyl, phenyl, hydroxyor C₁-C₆ alkoxy, then one R⁵ is other than halogen, C₁-C₆ alkyl, hydroxyor C₁-C₆ alkoxy.

[0116] Also of note are methods for controlling arthropods comprisingcontacting the arthropods or their environment with an arthropodicidallyeffective amount of a compound of Formula IV and insecticidalcompositions thereof.

[0117] Preferred methods for reasons of better activity are:

[0118] Preferred 1. Methods comprising compounds of Formula 1 wherein Jis a phenyl group substituted with 1 to 2 R⁵ and optionally substitutedwith 1 to 3 R⁶.

[0119] Preferred 2. Methods of Preferred 1 wherein

[0120] A and B are both O;

[0121] n is 1 to 2;

[0122] R¹ is H, C₁-C₄ alkyl, C₂-C₄ alkenyl, C₂-C₄ alkynyl, C₃-C₆cycloalkyl, C₂-C₆ alkylcarbonyl or C₂-C₆ alkoxycarbonyl;

[0123] R² is H, C₁-C₄ alkyl, C₂-C₄ alkenyl, C₂-C₄ alkynyl, C₃-C₆cycloalkyl, C₂-C₆ alkylcarbonyl or C₂-C₆ alkoxycarbonyl;

[0124] R³ is C₁-C₆ alkyl, C₂-C₆ alkenyl, C₂-C₆ alkynyl or C₃-C₆cycloalkyl each optionally substituted with one or more substituentsselected from the group consisting of halogen, CN, C₁-C₂ alkoxy, C₁-C₂alkylthio, C₁-C₂ alkylsulfinyl and C₁-C₂ alkylsulfonyl;

[0125] one of the R⁴ groups is attached to the phenyl ring at the2-position or 5-position, and said R⁴ is C₁-C₄ alkyl C₁-C₄ haloalkyl,halogen, CN, NO₂, C₁-C₄ alkoxy, C₁-C₄ haloalkoxy, C₁-C₄ alkylthio, C₁-C₄alkylsulfinyl, C₁-C₄ alkylsulfonyl, C₁-C₄ haloalkylthio, C₁-C₄haloalkylsulfinyl or C₁-C₄ haloalkylsulfonyl;

[0126] each R⁵ is independently C₁-C₄ haloalkyl, CN, NO₂, C₁-C₄haloalkoxy, C₁-C₄ alkylthio, C₁-C₄ alkylsulfinyl, C₁-C₄ alkylsulfonyl,C₁-C₄ haloalkylthio, C₁-C₄ haloalkylsulfinyl, C₁-C₄ haloalkylsulfonyl orC₂-C₄ alkoxycarbonyl; or

[0127] (R⁵)₂ when attached to adjacent carbon atoms can be takentogether as —OCF₂O—, —CF₂CF₂O— or —OCF₂CF₂O—; and

[0128] each R⁶ is independently H, halogen, C₁-C₄ alkyl, C₁-C₂ alkoxy orC₂-C₄ alkoxycarbonyl, or

[0129] each R⁶ is independently a phenyl or a 5- or 6-memberedheteroaromatic ring, each ring optionally substituted with C₁-C₄ alkyl,C₂-C₄ alkenyl, C₂-C₄ alkynyl, C₃-C₆ cycloalkyl, C₁-C₄ haloalkyl, C₂-C₄haloalkenyl, C₂-C₄ haloalkynyl, C₃-C₆ halocycloalkyl, halogen, CN, NO₂,C₁-C₄ alkoxy, C₁-C₄ haloalkoxy, C₁-C₄ alkylthio, C₁-C₄ alkylsulfinyl,C₁-C₄ alkylsulfonyl, C₁-C₄ alkylamino, C₂-C₈ dialkylamino, C₃-C₆cycloalkylamino, C₃-C₆ (alkyl)cycloalkylamino, C₂-C₄ alkylcarbonyl,C₂-C₆ alkoxycarbonyl, C₂-C₆ alkylaminocarbonyl, C₃-C₈dialkylaminocarbonyl or C₃-C₆ trialkylsilyl.

[0130] Preferred 3. Methods of Preferred 2 wherein

[0131] R¹ and R² are both H;

[0132] R³ is C₁-C₄ alkyl optionally substituted with halogen, CN, OCH₃,S(O)_(p)CH₃;

[0133] each R⁴ is independently H, CH₃, CF₃, OCF₃, OCHF₂, S(O)_(p)CF₃,S(O)_(p)CHF₂, CN or halogen;

[0134] each R⁵ is independently CF₃, OCF₃, OCHF₂, S(O)_(p)CF₃,S(O)_(p)CHF₂, OCH₂CF₃, OCF₂CHF₂, S(O)_(p)CH₂CF₃ or S(O)_(p)CF₂CHF₂;

[0135] each R⁶ is independently H, halogen or methyl; or phenyl,pyrazole, imidazole, triazole, pyridine or pyrimidine, each ringoptionally substituted with C₁-C₄ alkyl, C₁-C₄ haloalkyl, halogen or CN;and p1 is 0, 1 or 2.

[0136] Preferred 4. Methods of Preferred 3 wherein R³ is i-propyl ort-butyl.

[0137] Preferred 5. Methods comprising compounds of Formula 1 wherein Jis a 5- or 6-membered heteroaromatic ring optionally substituted with 1to 4 R⁷.

[0138] Preferred 6. Methods of Preferred 5 wherein

[0139] J is a 5- or 6-membered heteroaromatic ring selected from thegroup consisting of J-1, J-2, J-3, J-4 and J-5, each J optionallysubstituted with 1 to 3 R⁷

[0140] Q is O, S or NR⁷; and

[0141] W, X, Y and Z are independently N or CR⁷, provided that in J-4and J-5 at least one of W, X, Y or Z is N.

[0142] Preferred 7. Methods of Preferred 5 or Preferred 6 wherein

[0143] A and B are O;

[0144] n is 1 to 2;

[0145] R¹ is H, C₁-C₄ alkyl, C₂-C₄ alkenyl, C₂-C₄ alkynyl, C₂-C₆alkylcarbonyl or C₂-C₆ alkoxycarbonyl;

[0146] R² is H, C₁-C₄ alkyl, C₂-C₄ alkenyl, C₂-C₄ alkynyl, C₃-C₆cycloalkyl, C₂-C₆ alkylcarbonyl or C₂-C₆ alkoxycarbonyl;

[0147] R³ is H; or C₁-C₆ alkyl, C₂-C₆ alkenyl, C₂-C₆ alkynyl or C₃-C₆cycloalkyl each optionally substituted with one or more substituentsselected from the group consisting of halogen, CN, C₁-C₂ alkoxy, C₁-C₂alkylthio, C₁-C₂ alkylsulfinyl and C₁-C₂ alkylsulfonyl;

[0148] one of the R⁴ groups is attached to the phenyl ring at the2-position, and said R⁴ is C₁-C₄ alkyl, C₁-C₄ haloalkyl, halogen, CN,NO₂, C₁-C₄ alkoxy, C₁-C₄ haloalkoxy, C₁-C₄ alkylthio, C₁-C₄alkylsulfinyl, C₁-C₄ alkylsulfonyl, C₁-C₄ haloalkylthio, C₁-C₄haloalkylsulfinyl, or C₁-C₄ haloalkylsulfonyl; and

[0149] each R⁷ is independently H, C₁-C₄ alkyl, C₁-C₄ haloalkyl,halogen, CN, NO₂, C₁-C₄ haloalkoxy, C₁-C₄ alkylthio, C₁-C₄alkylsulfinyl, C₁-C₄ alkylsulfonyl, C₁-C₄ haloalkylthio, C₁-C₄haloalkylsulfinyl, C₁-C₄ haloalkylsulfonyl or C₂-C₄ alkoxycarbonyl; or aphenyl or a 5- or 6-membered heteroaromatic ring, each ring optionallysubstituted with C₁-C₄ alkyl, C₂-C₄ alkenyl, C₂-C₄ alkynyl, C₃-C₆cycloalkyl, C₁-C₄ haloalkyl, C₂-C₄ haloalkenyl, C₂-C₄ haloalkynyl, C₃-C₆halocycloalkyl, halogen, CN, NO₂, C₁-C₄ alkoxy, C₁-C₄ haloalkoxy, C₁-C₄alkylthio, C₁-C₄ alkylsulfinyl C₁-C₄ alkylsulfonyl, C₁-C₄ alkylamino,C₂-C₈ dialkylamino, C₃-C₆ cycloalkylamino, C₃-C₆ (alkyl)cycloalkylamino,C₂-C₄ alkylcarbonyl, C₂-C₆ alkoxycarbonyl, C₂-C₆ alkylaminocarbonyl,C₃-C₈ dialkylaminocarbonyl or C₃-C₆ trialkylsilyl.

[0150] Preferred 8. Methods of Preferred 7 wherein

[0151] J is selected from the group consisting of pyridine, pyrimidine,pyrazole, imidazole, triazole, thiophene, thiazole and oxazole, furan,isothiazole and isoxazole, each optionally substituted with 1 to 3 R⁷.

[0152] Preferred 9. Methods of Preferred 8 wherein

[0153] J is selected from the group consisting of pyridine, pyrimidine,pyrazole, thiophene and thiazole, each optionally substituted with 1 to3 R⁷;

[0154] R¹ and R² are both H;

[0155] R³ is C₁-C₄ alkyl optionally substituted with halogen, CN, OCH₃,S(O)_(p)CH₃;

[0156] each R⁴ is independently H, CH₃, CF₃, OCF₃, OCHF₂, S(O)_(p)CF₃,S(O)_(p)CHF₂, CN or halogen;

[0157] each R⁷ is independently H, halogen, CH₃, CF₃, OCHF₂,S(O)_(p)CF₃, S(O)_(p)CHF₂, OCH₂CF₃, OCF₂CHF₂, S(O)_(p)CH₂CF₃,S(O)_(p)CF₂CHF₂; or phenyl, pyrazole, imidazole, triazole, pyridine orpyrimidine, each ring optionally substituted with C₁-C₄ alkyl, C₁-C₄haloalkyl, C₁-C₄ alkoxy, C₁-C₄ haloalkoxy, C₁-C₄ alkylthio, C₁-C₄alkylsulfinyl, C₁-C₄ alkylsulfonyl, halogen or CN; and

[0158] p is 0, 1 or 2.

[0159] Preferred 10. Methods of Preferred 9 wherein J is a pyridineoptionally substituted with 1 to 3 R⁷.

[0160] Preferred 11. Methods of Preferred 10 wherein one R⁷ is a phenyloptionally substituted with C₁-C₄ alkyl, C₁-C₄ haloalkyl, halogen or CN.

[0161] Preferred 12. Methods of Preferred 10 wherein one R⁷ is apyrazole, imidazole, triazole, pyridine or pyrimidine, each ringoptionally substituted with C₁-C₄ alkyl, C₁-C₄ haloalkyl, halogen or CN.

[0162] Preferred 13. Methods of Preferred 9 wherein J is a pyrimidineoptionally substituted with 1 to 3 R⁷.

[0163] Preferred 14. Methods of Preferred 13 wherein one R⁷ is a phenyloptionally substituted with C₁-C₄ alkyl, C₁-C₄ haloalkyl, halogen or CN.

[0164] Preferred 15. Methods of Preferred 13 wherein one R⁷ is apyrazole, imidazole, triazole, pyridine or pyrimidine, each ringoptionally substituted with C₁-C₄ alkyl, C₁-C₄ haloalkyl, halogen or CN.

[0165] Preferred 16. Methods of Preferred 9 wherein J is a pyrazoleoptionally substituted with 1 to 3 R⁷.

[0166] Preferred 17. Methods of Preferred 16 wherein one R⁷ is a phenyloptionally substituted with C₁-C₄ alkyl, C₁-C₄ haloalkyl, halogen or CN.

[0167] Preferred 18. Methods of Preferred 16 wherein one R⁷ is apyrazole, imidazole, triazole, pyridine or pyrimidine, each ringoptionally substituted with C₁-C₄ alkyl, C₁-C₄ haloalkyl, halogen or CN.

[0168] Preferred 19. Methods of Preferred 18 wherein R⁷ is a pyridineoptionally substituted with C₁-C₄ alkyl, C₁-C₄ haloalkyl, halogen or CN.

[0169] Most preferred is the method comprising a compound of Formula 1selected from the group consisting of:

[0170]3-methyl-N-(1-methylethyl)-2-[[4-(trifluoromethyl)benzoyl]amino]-benzamide,

[0171]2-methyl-N-[2-methyl-6-[[(1-methylethyl)amino]carbonyl]phenyl]4-(trifluoromethyl)benzamide,

[0172]2-methyl-N-[2-methyl-6-[[(1-methylethyl)amino]carbonyl]phenyl]-6-(trifluoromethyl)-3-pyridinecarboxamide,

[0173]1-ethyl-N-[2-methyl-6-[[(1-methylethyl)amino]carbonyl]phenyl]-3-(trifluoromethyl)-1H-pyrazole-5-carboxamide,

[0174]1-(2-fluorophenyl)-N-[2-methyl-6-[[(1-methylethyl)amino)carbonyl]phenyl]-3-(trifluoromethyl)-1H-pyrazole-5-carboxamide,

[0175]1-(3-chloro-2-pyridinyl)-N-[2-methyl-6-[[(1-methylethyl)amino]carbonyl]phenyl]3-20(trifluoromethyl)-1H-pyrazole-5-carboxamide,

[0176]N-[2-chloro-6-[[(1-methylethyl)amino]carbonyl]phenyl]-1-(3-chloro-2-pyridinyl)-3-(trifluoromethyl)-1H-pyrazole-5-carboxamide,

[0177]3-bromo-1-(2-chlorophenyl)-N-[2-methyl-6-[[(1-methylethyl)amino]carbonyl]phenyl]-1H-pyrazole-5-carboxamide,and

[0178]3-bromo-N-[2-chloro-6-[[(1-methylethyl)amino]carbonyl]phenyl]-1-(2-chlorophenyl)-1H-pyrazole-5-carboxamide.

[0179] Preferred compounds for reasons of better activity and/or ease ofsynthesis are:

[0180] Preferred A. Compounds of Formula 1 wherein J is a phenyl groupsubstituted with 1 to 2 R⁵ and optionally substituted with 1 to 3 R⁶.

[0181] Preferred B. Compounds of Preferred A wherein

[0182] A and B are both O;

[0183] n is 1 to 2;

[0184] R¹ is H, C₁-C₄ alkyl, C₂-C₄ alkenyl, C₂-C₄ alkynyl, C₃-C₆cycloalkyl, C₂-C₆ alkylcarbonyl or C₂-C₆ alkoxycarbonyl;

[0185] R² is H, C₁-C₄ alkyl, C₂-C₄ alkenyl, C₂-C₄ alkyl, C₃-C₆cycloalkyl, C₂-C₆ alkylcarbonyl or C₂-C₆ alkoxycarbonyl;

[0186] R³ is C₁-C₆ alkyl, C₂-C₆ alkenyl, C₂-C₆ alkynyl or C₃-C₆cycloalkyl each optionally substituted with one or more substituentsselected from the group consisting of halogen, CN, C₁-C₂ alkoxy, C₁-C₂alkylthio, C₁-C₂ alkylsulfinyl and C₁-C₂ alkylsulfonyl;

[0187] one of the R⁴ groups is attached to the phenyl ring at the2-position or 5-position, and said R⁴ is C₁-C₄ alkyl, C₁-C₄ haloalkyl,halogen, CN, NO₂, C₁-C₄ alkoxy, C₁-C₄ haloalkoxy, C₁-C₄ alkylthio, C₁-C₄alkylsulfinyl, C₁-C₄ alkylsulfonyl, C₁-C₄ haloalkylthio, C₁-C₄haloalkylsulfinyl or C₁-C₄ haloalkylsulfonyl;

[0188] each R⁵ is independently C₁-C₄ haloalkyl, CN, NO₂, C₁-C₄haloalkoxy, C₁-C₄ alkylthio, C₁-C₄ alkylsulfinyl, C₁-C₄ alkylsulfonyl,C₁-C₄ haloalkylthio, C₁-C₄ haloalkylsulfinyl, C₁-C₄ haloalkylsulfonyl orC₂-C₄ alkoxycarbonyl; or

[0189] (R⁵)₂ when attached to adjacent carbon atoms can be takentogether as —OCF₂O—, —CF₂CF₂O— or —OCF₂CF₂O—; and

[0190] each R⁶ is independently H, halogen, C₁-C₄ alkyl, C₁-C₂ alkoxy orC₂-C₄ alkoxycarbonyl, or

[0191] each R⁶ is independently a phenyl or a 5- or 6-memberedheteroaromatic ring, each ring optionally substituted with C₁-C₄ alkyl,C₂-C₄ alkenyl, C₂-C₄ alkynyl, C₃-C₆ cycloalkyl, C₁-C₄ haloalkyl, C₂-C₄haloalkenyl, C₂-C₄ haloalkynyl, C₃-C₆ halocycloalkyl, halogen, CN, NO₂,C₁-C₄ alkoxy, C₁-C₄ haloalkoxy, C₁-C₄ alkylthio, C₁-C₄ alkylsulfinyl,C₁-C₄ alkylsulfonyl, C₁-C₄ alkylamino, C₂-C₈ dialkylamino, C₃-C₆cycloalkylamino, C₃-C₆ (alkyl)cycloalkylamino, C₂-C₄ alkylcarbonyl,C₂-C₆ alkoxycarbonyl, C₂-C₆ alkylaminocarbonyl, C₃-C₈dialkylaminocarbonyl or C₃-C₆ trialkylsilyl.

[0192] Preferred C. Compounds of Preferred B wherein

[0193] R¹ and R² are both H;

[0194] R³ is C₁-C₄ alkyl optionally substituted with halogen, CN, OCH₃,S(O)_(p)CH₃;

[0195] each R⁴ is independently H, CH₃, CF₃, OCF₃, OCHF₂, S(O)_(p)CF₃,S(O)_(p)CHF₂, CN or halogen;

[0196] each R⁵ is independently CF₃, OCF₃, OCHF₂, S(O)_(p)CF₃,S(O)_(p)CHF₂, OCH₂CF₃, OCF₂CHF₂, S(O)_(p)CH₂CF₃ or S(O)_(p)CF₂CHF₂;

[0197] each R⁶ is independently H, halogen or methyl; or phenyl,pyrazole, imidazole, triazole, pyridine or pyrimidine, each ringoptionally substituted with C₁-C₄ alkyl, C₁-C₄ haloalkyl, halogen or CN;and

[0198] p is 0, 1 or 2.

[0199] Preferred D. Compounds of Preferred C wherein R³ is i-propyl ort-butyl.

[0200] Preferred E. Compounds of Formula 1 wherein J is a 5- or6-membered heteroaromatic ring is optionally substituted with 1 to 4 R⁷.

[0201] Preferred F. Compounds of Preferred E wherein

[0202] J is a 5- or 6-membered heteroaromatic ring selected from thegroup consisting of J-1, J-2, J-3, J-4 and J-5, each J optionallysubstituted with 1 to 3 R⁷

[0203] Q is O, S or NR⁷; and

[0204] W, X, Y and Z are independently N or CR⁷, provided that in J-4and J-5 at least one of W, X, Y or Z is N.

[0205] Preferred G. Compounds of Preferred E or Preferred F wherein

[0206] A and B are O;

[0207] n is 1 to 2;

[0208] R¹ is H, C₁-C₄ alkyl, C₂-C₄ alkenyl, C₂-C₄ alkynyl, C₂-C₆alkylcarbonyl or C₂-C₆ alkoxycarbonyl;

[0209] R² is H, C₁-C₄ alkyl, C₂-C₄ alkenyl, C₂-C₄ alkynyl, C₃-C₆cycloalkyl, C₂-C₆ alkylcarbonyl or C₂-C₆ alkoxycarbonyl;

[0210] R³ is H; or C₁-C₆ alkyl, C₂-C₆ alkenyl, C₂-C₆ alkynyl or C₃-C₆cycloalkyl each optionally substituted with one or more substituentsselected from the group consisting of halogen, CN, C₁-C₂ alkoxy, C₁-C₂alkylthio, C₁-C₂ alkylsulfinyl and C₁-C₂ alkylsulfonyl;

[0211] one of the R⁴ groups is attached to the phenyl ring at the2-position, and said R⁴ is C₁-C₄ alkyl, C₁-C₄ haloalkyl, halogen, CN,NO₂, C₁-C₄ alkoxy, C₁-C₄ haloalkoxy, C₁-C₄ alkylthio, C₁-C₄alkylsulfinyl, C₁-C₄ alkylsulfonyl, C₁-C₄ haloalkylthio, C₁-C₄haloalkylsulfinyl or C₁-C₄ haloalkylsulfonyl; and

[0212] each R⁷ is independently H, C₁-C₄ alkyl, C₁-C₄ haloalkyl,halogen, CN, NO₂, C₁-C₄ haloalkoxy, C₁-C₄ alkylthio, C₁-C₄alkylsulfinyl, C₁-C₄ alkylsulfonyl, C₁-C₄ haloalkylthio, C₁-C₄haloalkylsulfinyl, C₁-C₄ haloalkylsulfonyl or C₂-C₄ alkoxycarbonyl; or aphenyl or a 5- or 6-membered heteroaromatic ring, each ring optionallysubstituted with C₁-C₄ alkyl, C₂-C₄ alkenyl, C₂-C₄ alkynyl, C₃-C₆cycloalkyl, C₁-C₄ haloalkyl, C₂-C₄ haloalkenyl, C₂-C₄ haloalkynyl, C₃-C₆halocycloalkyl, halogen, CN, NO₂, C₁-C₄ alkoxy, C₁-C₄ haloalkoxy, C₁-C₄alkylthio, C₁-C₄ alkylsulfinyl, C₁-C₄ alkylsulfonyl, C₁-C₄ alkylamino,C₂-C₈ dialkylamino, C₃-C₆ cycloalkylamino, C₃-C₆ (alkyl)cycloalkylamino,C₂-C₄ alkylcarbonyl, C₂-C₆ alkoxycarbonyl, C₂-C₆ alkylaminocarbonyl,C₃-C₈ dialkylaminocarbonyl or C₃-C₆ trialkylsilyl.

[0213] Preferred H. Compounds of Preferred G wherein

[0214] J is selected from the group consisting of pyridine, pyrimidine,pyrazole, imidazole, triazole, thiophene, thiazole and oxazole, furan,isothiazole and isoxazole, each optionally substituted with 1 to 3 R⁷.

[0215] Preferred I. Compounds of Preferred H wherein

[0216] J is selected from the group consisting of pyridine, pyrimidine,pyrazole, thiophene and thiazole, each optionally substituted with 1 to3 R⁷;

[0217] R¹ and R² are both H;

[0218] R³ is C₁-C₄ alkyl optionally substituted with halogen, CN, OCH₃,S(O)_(p)CH₃;

[0219] each R⁴ is independently H, CH₃, CF₃, OCF₃, OCHF₂, S(O)_(p)CF₃,S(O)_(p)CHF₂, CN or halogen;

[0220] each R⁷ is independently H, halogen, CH₃, CF₃, OCHF₂,S(O)_(p)CF₃, S(O)_(p)CHF₂, OCH₂CF₃, OCF₂CHF₂, S(O)_(p)CH₂CF₃,S(O)_(p)CF₂CHF₂; or phenyl, pyrazole, imidazole, triazole, pyridine orpyrimidine, each ring optionally substituted with C₁-C₄ alkyl, C₁-C₄haloalkyl, C₁-C₄ alkoxy, C₁-C₄ haloalkoxy, C₁-C₄ alkylthio, C₁-C₄alkylsulfinyl, C₁-C₄ alkylsulfonyl, halogen or CN; and

[0221] p is 0, 1 or 2.

[0222] Preferred J. Compounds of Preferred I wherein J is a pyridineoptionally substituted with 1 to 3 R⁷.

[0223] Preferred K. Compounds of Preferred J wherein one R⁷ is a phenyloptionally substituted with C₁-C₄ alkyl, C₁-C₄ haloalkyl, halogen or CN.

[0224] Preferred L. Compounds of Preferred J wherein one R⁷ is apyrazole, imidazole, triazole, pyridine or pyrimidine, each ringoptionally substituted with C₁-C₄ alkyl, C₁-C₄ haloalkyl, halogen or CN.

[0225] Preferred M. Compounds of Preferred I wherein J is a pyrimidineoptionally substituted with 1 to 3 R⁷.

[0226] Preferred N. Compounds of Preferred M wherein one R⁷ is a phenyloptionally substituted with C₁-C₄ alkyl, C₁-C₄ haloalkyl, halogen or CN.

[0227] Preferred O. Compounds of Preferred M wherein one R⁷ is apyrazole, imidazole, triazole, pyridine or pyrimidine, each ringoptionally substituted with C₁-C₄ alkyl, C₁-C₄ haloalkyl, halogen or CN.

[0228] Preferred P. Compounds of Preferred I wherein J is a pyrazoleoptionally substituted with 1 to 3 R⁷.

[0229] Preferred Q. Compounds of Preferred P wherein one R⁷ is a phenyloptionally substituted with C₁-C₄ alkyl, C₁-C₄ haloalkyl, halogen or CN.

[0230] Preferred R. Compounds of Preferred P wherein one R⁷ is apyrazole, imidazole, triazole, pyridine or pyrimidine, each ringoptionally substituted with C₁-C₄ alkyl, C₁-C₄ haloalkyl, halogen or CN.

[0231] Preferred S. Compounds of Preferred R wherein R⁷ is a pyridineoptionally substituted with C₁-C₄ alkyl, C₁-C₄ haloalkyl, halogen or CN.

[0232] Most preferred is the compound of Formula 1 selected from thegroup consisting of:

[0233]3-methyl-N-(1-methylethyl)-2-[[4-(trifluoromethyl)benzoyl]amino]-benzamide,

[0234] 2-methyl-N-[2-methyl-6-[[(1-methylethyl)amino]carbonyl]phenyl]-4(trifluoromethyl)benzamide,

[0235]2-methyl-N-[2-methyl-6-[[(1-methylethyl)amino]carbonyl]phenyl]-6-(trifluoromethyl)-3-pyridinecarboxamide,

[0236]1-ethyl-N-[2-methyl-6-[[(1-methylethyl)amino]carbonyl]phenyl]-3-(trifluoromethyl)-1H-pyrazole-5-carboxamide,

[0237]1-(2-fluorophenyl)-N-[2-methyl-6-[[(1-methylethyl)amino)carbonyl]phenyl]-3-(trifluoromethyl)-1H-pyrazole-5-carboxaride,

[0238]1-(3-chloro-2-pyridinyl)-N-[2-methyl-6-[[(1-methylethyl)amino]carbonyl]phenyl]3-(trifluoromethyl)-1H-pyrarzole-5-carboxamide,

[0239]N-[2-chloro-6-[[(1-methylethyl)amino]carbonyl]phenyl]-1-(3-chloro-2-pyridinyl)-3-(trifluoromethyl)-1H-pyrazole-5-carboxamide,

[0240]3-bromo-1-(2-chlorophenyl)-N-[2-methyl-6-[[(1-methylethyl)amino]carbonyl]phenyl]-1H-pyrazole-5-carboxamide,and

[0241]3-bromo-N-[2-chloro-6-[[(1-methylethyl)amino]carbonyl]phenyl]-1-(2-chlorophenyl)-1H-pyrazole-5-carboxamide.

[0242] Preferred compositions are those comprising compounds of formula1 as preferred in Preferred 1 through 19, and the specifically preferredcompounds above.

[0243] As noted above, each J is independently a phenyl group or anaphthyl group substituted with 1 to 2 R⁵ and optionally substitutedwith 1 to 3 R⁶; or each J is independently a 5- or 6-memberedheteroaromatic ring or an aromatic 8-, 9- or 10-membered fusedheterobicyclic ring system wherein each ring or ring system isoptionally substituted with 1 to 4 R⁷. The term “optionally substituted”in connection with these J groups refers to groups which areunsubstituted or have at least one non-hydrogen substituent that doesnot extinguish the arthropodicidal activity possessed by theunsubstituted analog. Note also that J-1 through J-5 above denote 5- or6-membered heteroaromatic rings. An example of phenyl substituted with 1to 2 R⁵ and optionally substituted with 1 to 3 R⁶ is the ringillustrated as J-6 in Exhibit 1, wherein m is an integer from 1-2 and qis an integer from 1 to 3. Note that at least one R⁵ must be present inJ-6. Although R⁶ groups are shown in the structure J-6, it is noted thatthey do not need to be present since they are optional substituents. Anexample of a naphthyl group substituted with 1 to 2 R⁵ and optionallysubstituted with 1 to 3 R⁶ is J-59 illustrated in Exhibit 1, wherein mis an integer from 1-2 and q is an integer from 1 to 3. Note that atleast one R⁵ must be present in J-59. Although R⁶ groups are shown inthe structure J-59, it is noted that they do not need to be presentsince they are optional substituents. Examples of 5- or 6-memberedheteroaromatic ring optionally substituted with 1 to 4 R⁷ include therings J-7 through J-58 illustrated in Exhibit 1 wherein r is an integerfrom 1 to 4. Note that J-7 through J-26 are examples of J-1, J-27through J41 are examples of J-2, J-42 through J-44 are examples of J-3,J-46 through J-53 are examples of J-4 and J-54 through J-58 are examplesof J-5. The nitrogen atoms that require substitution to fill theirvalence are substituted with R⁷. Note that some J groups can only besubstituted with less than 4 R⁷ groups (e.g. J-19, J-20, J-23 throughJ-26 and J-37 through J-40 can only be substituted with one R⁷).Examples of aromatic 8-, 9- or 10-membered fused heterobicyclic ringsystems optionally substituted with 1 to 4 R⁷ include J-60 through J-90illustrated in Exhibit 1 wherein r is an integer from 1 to 4. AlthoughR⁷ groups are shown in the structures J-7 through J-58 and J-60 throughJ-90, it is noted that they do not need to be present since they areoptional substituents. Note that when R⁵, R6 and/or R⁷ are H whenattached to an atom, this is the same as if said atom is unsubstituted.Note that when the attachment point between (R⁵)_(m), (R⁶)_(q) or(R⁷)_(r) and the J group is illustrated as floating, (R⁵)_(m), (R⁶)_(q)or (R⁷)_(r) can be attached to any available carbon atom of the J group.Note that when the attachment point on the J group is illustrated asfloating, the J group can be attached to the remainder of Formula 1through any available carbon of the J group by replacement of a hydrogenatom.

[0244] As noted above, G is a 5- or 6-membered nonaromatic carbocyclicor heterocyclic ring, optionally including one or two ring membersselected from the group consisting of C(═O), SO or S(O)₂ and optionallysubstituted with 1 to 4 substituents selected from the group consistingof C₁-C₂ alkyl, halogen, CN, NO₂ and C₁-C₂ alkoxy. The term “optionallysubstituted” in connection with these G groups refers to groups whichare unsubstituted or have at least one non-hydrogen substituent thatdoes not extinguish the arthropodicidal activity possessed by theunsubstituted analog. Note that when the attachment point on the G groupis illustrated as floating, the G group can be attached to the remainderof Formula 1 through any available carbon of the G group by replacementof a hydrogen atom. The optional substituents can be attached to anyavailable carbon by replacing a hydrogen atom. Examples of 5- or6-membered nonaromatic carbocyclic rings as G include the ringsillustrated as G-1 through G-8 of Exhibit 2, wherein such rings areoptionally substituted with 1 to 4 substituents selected from the groupconsisting of C₁-C₂ alkyl, halogen, CN, NO₂ and C₁-C₂ alkoxy. Examplesof 5- or 6-membered nonaromatic heterocyclic rings as G include therings illustrated as G-9 through G-48 of Exhibit 2, wherein such ringsare optionally substituted with 1 to 4 substituents selected from thegroup consisting of C₁-C₂ alkyl, halogen, CN, NO₂ and C₁-C₂ alkoxy. Notethat when G comprises a ring selected from G-31 through G-34, G-37 andG-38, Q¹ is selected from O, S or N. Note that when G is G-11, G13,G-14, G16, G-23, G-24, G-30 through G-34, G-37 and G-38 and Q¹ is N, thenitrogen atom can complete its valence by substitution with either H orC₁-C₂ alkyl.

[0245] As noted above, each R⁶ and each R⁷ can be independently (amongothers) 5- or 6-membered heteroaromatic rings or aromatic 8-, 9- or10-membered fused heterobicyclic ring systems, each ring optionallysubstituted with one to three substituents independently selected fromthe group consisting of C₁-C₄ alkyl, C₂-C₄ alkenyl, C₂-C₄ alkynyl, C₃-C₆cycloalkyl, C₁-C₄ haloalkyl, C₂-C₄ haloalkenyl, C₂-C₄ haloalkynyl, C₃-C₆halocycloalkyl, halogen, CN, NO₂, C₁-C₄ alkoxy, C₁-C₄ haloalkoxy, C₁-C₄alkylthio, C₁-C₄ alkylsulfinyl, C₁-C₄ alkylsulfonyl, C₁-C₄ alkylamino,C₂-C₈ dialkylamino, C₃-C₆ cycloalkylamino, C₃-C₆ (alkyl)cycloalkylamino,C₂-C₄ alkylcarbonyl, C₂-C₆ alkoxycarbonyl, C₂-C₆ alkylaminocarbonyl,C₃-C₈ dialkylaminocarbonyl or C₃-C₆ trialkylsilyl. Examples of such R⁶and R⁷ groups include the rings or ring systems illustrated as rings J-7through J-58 and J-60 through J-90 illustrated in Exhibit 1, except thatsuch rings are optionally substituted with 1 to 3 substituents selectedfrom the group consisting of C₁-C₄ alkyl, C₂-C₄ alkenyl, C₂-C₄ alkynyl,C₃-C₆ cycloalkyl, C₁-C₄ haloalkyl, C₂-C₄ haloalkenyl, C₂-C₄ haloalkynyl,C₃-C₆ halocycloalkyl, halogen, CN, NO₂, C₁-C₄ alkoxy, C₁-C₄ haloalkoxy,C₁-C₄ alkylthio C₁-C₄ alkylsulfinyl, C₁-C₄ alkylsulfonyl, C₁-C₄alkylamino, C₂-C₈ dialkylamino, C₃-C₆ cycloalkylamino, C₃-C₆(alkyl)cycloalkylamino, C₂-C₄ alkylcarbonyl, C₂-C₆ alkoxycarbonyl, C₂-C₆alkylaminocarbonyl, C₃-C₈ dialkylaminocarbonyl or C₃-C₆ trialkylsilylrather than (R⁷)_(r). Note that these substituents can be attached toany available carbon atom of the J group by replacement of a hydrogenatom. Note that when the attachment point on the J group is illustratedas floating, the J group can be attached to the remainder of Formula 1through any available carbon of the J group by replacement of a hydrogenatom.

[0246] One or more of the following methods and variations as describedin Schemes 1-17 can be used to prepare the compounds of Formula 1. Thedefinitions of A, B, J, R¹, R², R³, R⁴, R⁵, R⁶, R⁷, m and n in thecompounds of Formulae 1-34 below are as defined above in the Summary ofthe Invention. Compounds of Formulae 1a-c, 2a-b, 4a-g, 5a-b are varioussubsets of the compounds of Formula 1, 2, 4 and 5.

[0247] Compounds of Formula 1 can be prepared by procedures outlined inSchemes 1-17. A typical procedure is detailed in Scheme 1 and involvescoupling of an anthranilic amide of Formula 2 with an acid chloride ofFormula 3 in the presence of an acid scavenger to provide the compoundof Formula 1a. Typical acid scavengers include amine bases such astriethylamine, diisopropylethylamine and pyridine; other scavengersinclude hydroxides such as sodium and potassium hydroxide and carbonatessuch as sodium carbonate and potassium carbonate. In certain instancesit is useful to use polymer-supported acid scavengers such aspolymer-bound diisopropylethylamine and polymer-bounddimetliylaminopyridine. In a subsequent step, amides of Formula 1a canbe converted to thioamides of Formula 1b using a variety of standardthio transfer reagents including phosphorus pentasulfide and Lawesson'sreagent.

[0248] An alternate procedure for the preparation of compounds ofFormula 1a involves coupling of an anthranilic amide of Formula 2 withan acid of Formula 4 in the presence of a dehydrating agent such asdicyclohexylcarbodiimide (DCC). Polymer supported reagents are againuseful here, such as polymer-bound cyclohexylcarbodiimide. Syntheticprocedures of Schemes 1 and 2 are only representative examples of usefulmethods for the preparation of Formula 1 compounds as the syntheticliterature is extensive for this type of reaction.

[0249] One skilled in the art will also realize that acid chlorides ofFormula 3 may be prepared from acids of Formula 4 by numerous well-knownmethods.

[0250] Anthranilic amides of Formula 2a are typically available from thecorresponding 2-nitrobenzamides of Formula 5 via catalytic hydrogenationof the nitro group. Typical procedures involve reduction with hydrogenin the presence of a metal catalyst such as palladium on carbon orplatinum oxide and in hydroxylic solvents such as ethanol andisopropanol. These procedures are well documented in the chemicalliterature. R¹ substituents such as alkyl, substituted alkyl and thelike can generally be introduced at this stage through known proceduresincluding either direct alkylation or through the generally preferredmethod of reductive alkylation of the amine. A commonly employedprocedure is to combine the aniline 2a with an aldehyde in the presenceof a reducing agent such as sodium cyanoborohydride to produce theFormula 2b compounds where R¹ is alkyl, alkenyl, alkynyl or substitutedderivatives thereof.

[0251] The intermediate amides of Formula 5a are readily prepared fromcommercially available 2-nitrobenzoic acids. Typical methods for amideformation can be applied here. These include direct dehydrative couplingof acids of Formula 6 with amines of Formula 7 using for example DCC,and conversion of the acids to an activated form such as the acidchlorides or anhydrides and subsequent coupling with amines to formamides of Formula 5a. We have found ethylchloroformate to be anespecially useful reagent for this type of reaction involving activationof the acid. The chemical literature is extensive on this type ofreaction. Amides of Formula 5a are readily converted to thioamides ofFormula 5b by using commercially available thio transfer reagents suchas phosphorus pentasulfide and Lawesson's reagent.

[0252] Benzoic acids of Formula 4 (J is optionally substituted phenyl)are generally well known in the art as are procedures for theirpreparation. One particularly useful subset of benzoic acids of thisinvention are 2-methyl-4-perfluoroalkyl benzoic acids of Formula 4a (R⁵equals e.g. CF₃, C₂F₅, C₃F₇). The synthesis for these compounds isoutlined in Schemes 5-9. Benzoic acids of Formula 4a may be preparedfrom the benzonitriles of Formula 8 by hydrolysis. The conditions usedmay involve the use of a base such as an alkaline metal hydroxide oralkoxide (e.g. potassium or sodium hydroxide) in a solvent such aswater, ethanol or ethylene glycol (e.g. J. Chem. Soc. 1948, 1025).Alternatively, the hydrolysis may be carried out using an acid such assulfuric acid or phosphoric acid in a suitable solvent such as water(e.g. Org. Synth. 1955, Coll vol. 3, 557). The choice of the conditionsis contingent on the stability of R⁵ to the reaction conditions andelevated temperatures are usually employed to achieve thistransformation.

[0253] Nitriles of Formula 8 may be prepared from anilines of Formula 9by the classical sequence involving diazotization and treatment of theintermediate diazonium salt with a copper cyanide salt (e.g. J. Amer.Chem. Soc. 1902, 24, 1035).

[0254] Anilines of Formula 9 may be prepared from compounds of Formula10. This transformation may be achieved by a well-known procedure thatemploys Raney Nickel (Org. Synth. Coll. Vol VI, 581). Alternatively, thesame transformation may be effected by the use of a suitable catalystsuch as palladium in the presence of hydrogen. The reaction is usuallyconducted at pressures of 10² to 10⁵ kPa in a suitable organic solventsuch as, but not limited to, toluene. Elevated temperatures of 80-110°C. are usually required to achieve the transformation. As one skilled inthe art will realize, numerous chemical modifications of the thioethermoiety are possible, and may be employed when necessary to facilitatethis transformation.

[0255] Compounds of Formula 10 may be prepared from iminosulfuranes ofFormula 11. The transformation may be achieved in a protic solvent suchas methanol or water, in a non-protic solvent such as dichloromethane ortoluene in the presence of a suitable base such as triethylamine (e.g.Org. Synth. Coll. Vol. VI, 581) or sodium methoxide, or in a combinationof a protic solvent, a protic solvent and a base. The temperature atwhich the reaction is conducted is usually in the range 40-110° C. Asone skilled in the art will realize, suitable salts of compounds ofFormula 11 such as, but not limited to a hydrochloride, a sulfate or abisulfate may also be employed, provided that the appropriate amount ofbase is first used to generate the free base 11. This may be done as aseparate step or as an integral part of the step involving thetransformation of compounds of Formula 11 to compounds of Formula 10.

[0256] Compounds of Formula 11 may be prepared from anilines of Formula12 by reaction with dimethyl sulfide and a suitable chlorinating agentsuch as, but not limited to N-chlorosuccinimide (e.g. Org. Synth. Coll.Vol. VI, 581), chlorine or N-chlorobenzotriazole. Alternatively,anilines of Formula 12 may be treated with dimethyl sulfoxide which hasbeen “activated” by treatment with an agent such as acetic anhydride,trifluoroacetic, anhydride, trifluoromethanesulfonic anhydride,cyclohexylcarbodiimide, sulfur trioxide, or phosphorus pentoxide. Thereaction is conducted in a suitable organic solvent such asdichloromethane or dimethyl sulfoxide. The reaction is conducted at atemperature of −70° C. to 25° C. and is dependent on the solvent andreagent used.

[0257] Intermediate anthranilic amides of Formula 2a and 2b may also beprepared from isatoic anhydrides of Formula 13 and 14 (Scheme 10).Typical procedures involve combination of equimolar amounts of the amine7 with the isatoic anhydride in polar aprotic solvents such as pyridineand dimethylformamide at temperatures ranging from room temperature to100° C. R¹ substituents such as alkyl and substituted alkyl may beintroduced by the base catalyzed alkylation of isatoic anhydride 13 withknown alkylating reagents R¹-Lg (wherein Lg is a leaving group such ashalogen, alkyl or aryl suphonates or alkyl sulfates) to provide thealkyl substituted intermediates 14. Isatoic anhydrides of Formula 13 maybe made by methods described in Coppola, Synthesis 505-36 (1980).

[0258] An alternate procedure for the preparation of specific compoundsof Formula 1 (where A is O, B is O and R¹ is H) involves reaction of anamine 7 with a benzoxazinone of Formula 15. Typical procedures involvecombination of the amine with the benzoxazinone in solvents such astetrahydrofuran or pyridine at temperatures ranging from roomtemperature to the reflux temperature of the solvent. Benzoxazinones arewell documented in the chemical literature and are available via knownmethods that involve the coupling of either an anthranilic acid or anisatoic anhydride with an acid chloride. For references to the synthesisand chemistry of Benzoxazinones see Jakobsen et al, Biorganic andMedicinal Chemistry, 2000, 8, 2095-2103 and references cited within. Seealso Coppola, J. Heterocyclic Chemistry, 1999, 36, 563-588.

[0259] Heterocyclic acids 4, where J is equal to an optionallysubstituted heterocycle, can be prepared by procedures outlined inSchemes 12-17. Both general and specific references to a wide variety ofheterocyclic acids including thiophenes, furans, pyridines, pyrimidines,triazoles, imidazoles, pyrazoles, thiazoles, oxazoles, isothiazoles,thiadiazoles, oxadiazoles, triazines, pyrazines, pyridazines, andisoxazoles can be found in the following compendia: Rodd's Chemistry ofChemistry of Carbon Compounds, Vol. IVa to IVl., S. Coffey editor,Elsevier Scientific Publishing, New York, 1973; ComprehensiveHeterocyclic Chemistry, Vol. 1-7, A. R. Katritzky and C. W. Reeseditors, Pergamon Press, New York, 1984; Comprehensive HeterocyclicChemistry II, Vol. 1-9, A. R. Katritzky, C. W. Rees, and E. F. Scriveneditors, Pergamon Press, New York, 1996; and the series, The Chemistryof Heterocyclic Compounds, E. C. Taylor, editor, Wiley, New York.Particularly useful heterocyclic acids of this invention includepyridine acids, pyrimidine acids and pyrazole acids. Procedures for thesynthesis of representative examples of each are detailed in Schemes12-17. A variety of heterocyclic acids and general methods for theirsynthesis may be found in World Patent Application WO 98/57397.

[0260] The synthesis of representative pyridine acids (4b) is depictedin Scheme 12. This procedure involves the known synthesis of pyridinesfrom ,β-ketoesters and 4-aminobutenones (19). Substituent groups R⁷(a)and R⁷(b) include e.g. alkyl and haloalkyl.

[0261] The synthesis of representative pyrimidine acids (4c) is depictedin Scheme 13. This procedure involves the known synthesis of pyrimidinesfrom vinylidene-β-ketoesters (22) and amidines. Substituent groups R⁷(a)and R⁷(b) include e.g. alkyl and haloalkyl.

[0262] The synthesis of representative pyrazole acids (4d-4g) isdepicted in Schemes 14-17. Pyrazoles 4d are described in Scheme 14. Thesynthesis of Scheme 14 involves as the key step introduction of theR⁷(b) substituent via alkylation of the pyrazole. The alkylating agentR⁷(b)-Lg (wherein Lg is a leaving group such as Cl, Br, I, sulfonatessuch as p-toluenesulfonate or methanesulfonate or sulfates such as—SO₂OR⁷(b)) includes R⁷(b) groups such as C₁-C₆ alkyl, C₂-C₆ alkenyl,C₂-C₆ alkynyl, C₃-C₆ cycloalkyl, C₁-C₆ haloalkyl, C₂-C₆ haloalkenyl,C₂-C₆ haloalkynyl, C₃-C₆ halocycloalkyl, C₂-C₆ alkylcarbonyl, C₂-C₆alkoxycarbonyl, C₃-C₈ dialkylaminocarbonyl, C₃-C₆ trialkylsilyl; orphenyl, benzyl, benzoyl, 5- or 6-membered heteroaromatic ring or anaromatic 8-, 9- or 10-membered fused heterobicyclic ring system, eachring or ring system optionally substituted. Oxidation of the methylgroup affords the pyrazole carboxylic acid. Some of the more preferredR⁷(a) groups include haloalkyl.

[0263] Pyrazoles 4e are described in Scheme 15. These pyrazole acids maybe prepared via metallation and carboxylation of pyrazoles of formula 28as the key step. The R⁷(b) group is introduced in a manner similar tothat of Scheme 14, i.e. via alkylation with a R⁷(b) alkylating agent.Representative R⁷(a) groups include e.g. cyano, and haloalkyl.

[0264] Pyrazoles 4f are described in Scheme 16. These can be preparedvia reaction of an optionally substituted phenyl hydrazine 29 with apyruvate 30 to yield pyrazole esters 31. Hydrolysis of the ester affordsthe pyrazole acids 4f. This procedure is particularly useful for thepreparation of compounds where R⁷(b) is optionally substituted phenyland R⁷(a) is haloalkyl.

[0265] Pyrazoles acids of Formula 4g are described in Scheme 17. Thesecan be prepared via 3+2 cycloaddition of an appropriately substitutednitrilimine with either substituted propiolates (33) or acrylates (36).Cycloaddition with acrylates requires additional oxidation of theintermediate pyrazoline to the pyrazole. Hydrolysis of the ester affordsthe pyrazole acids 4g. Preferred iminohalides for this reaction includethe trifluoromethyl iminochloride (38) and the iminodibromide (39).Compounds such as 38 are known (J. Heterocycl. Chem. 1985, 22(2),565-8). Compounds such as 39 are available by known methods (TetrahedronLetters 1999, 40, 2605). These procedures are particularly useful forthe preparation of compounds where R⁷(b) is optionally substitutedphenyl and R⁷(a) is haloalkyl or bromo.

[0266] It is recognized that some reagents and reaction conditionsdescribed above for preparing compounds of Formula I may not becompatible with certain functionalities present in the intermediates. Inthese instances, the incorporation of protection/deprotection sequencesor functional group interconversions into the synthesis will aid inobtaining the desired products. The use and choice of the protectinggroups will be apparent to one skilled in chemical synthesis (see, forexample, Greene, T. W.; Wuts, P. G. M. Protective Groups in OrganicSynthesis, 2nd ed.; Wiley: New York, 1991). One skilled in the art willrecognize that, in some cases, after the introduction of a given reagentas it is depicted in any individual scheme, it may be necessary toperform additional routine synthetic steps not described in detail tocomplete the synthesis of compounds of Formula 1. One skilled in the artwill also recognize that it may be necessary to perform a combination ofthe steps illustrated in the above schemes in an order other than thatimplied by the particular sequence presented to prepare the compounds ofFormula 1.

[0267] One skilled in the art will also recognize that compounds ofFormula 1 and the intermediates described herein can be subjected tovarious electrophilic, nucleophilic, radical, organometallic, oxidation,and reduction reactions to add substituents or modify existingsubstituents.

[0268] Without further elaboration, it is believed that one skilled inthe art using the preceding description can utilize the presentinvention to its fullest extent. The following Examples are, therefore,to be construed as merely illustrative, and not limiting of thedisclosure in any way whatsoever. Percentages are by weight except forchromatographic solvent mixtures or where otherwise indicated. Parts andpercentages for chromatographic solvent mixtures are by volume unlessotherwise indicated. ¹H NMR spectra are reported in ppm downfield fromtetramethylsilane; s is singlet, d is doublet, t is triplet, q isquartet, m is multiplet, dd is doublet of doublets, dt is doublet oftriplets, br s is broad singlet.

EXAMPLE 1

[0269] Step A: Preparation of3-methyl-N-(1-methylethyl)-2-nitrobenzamide

[0270] A solution of 3-methyl-2-nitrobenzoic acid (2.00 g, 11.0 mmol)and triethylamine (1.22 g, 12.1 mmol) in 25 mL of methylene chloride wascooled to 10° C. Ethyl chloroformate was carefully added and a solidprecipitate formed. After stirring for 30 minutes isopropylamine (0.94g, 16.0 mmol) was added and a homogeneous solution resulted. Thereaction was stirred for an additional hour, poured into water andextracted with ethyl acetate. The organic extracts were washed withwater, dried over magnesium sulfate and evaporated under reducedpressure to afford 1.96 g of the desired intermediate as a white solidmelting at 126-128° C.

[0271]¹H NMR (CDCl₃) δ 1.24 (d,6H), 2.38 (s,3H), 4.22 (m,1H), 5.80 (brs,1H), 7.4 (m,3H).

[0272] Step B: Preparation of2-amino-3-methyl-N-(1-methylethyl)benzamide

[0273] The 2-nitrobenzamide of Step A (1.70 g, 7.6 mmol) washydrogenated over 5% Pd/C in 40 mL of ethanol at 50 psi. When the uptakeof hydrogen ceased the reaction was filtered through celite and thecelite was washed with ether. The filtrate was evaporated under reducedpressure to afford 1.41 g of the title compound as a solid melting at149-151° C.

[0274]¹H NMR (CDCl₃) δ 1.24 (dd,6H), 2.16 (s,3H), 4.25 (m,1H), 5.54 (brs,2H), 5.85 (br s,1H), 6.59 (t,1H), 7.13 (d,1H), 7.17 (d,1H).

[0275] Step C: Preparation of3-methyl-N-(1-methylethyl)-2-[[4-(trifluoromethoxy)benzoyl]amino]benzamide

[0276] 4-(trifluoromethoxy)benzoyl chloride (0.29 g, 1.3 mmol) was addeddropwise to a mixture of the aniline from Step B (0.25 g, 1.3 mmol) andtriethylamine (0.13 g, 1.3 mmol) in 5 mL of methylene chloride at roomtemperature. After stirring for one hour the reaction was poured intowater and extracted with ethyl acetate. The combined extracts were driedover magnesium sulfate and evaporated under reduced pressure. Theresulting solids were washed with hexane/ether and filtered to afford0.41 g of the title compound, a compound of the present invention, as asolid melting at 207-209° C.

[0277]¹H NMR (CDCl₃) 67 1.19 (d, 6H), 2.33 (s, 3H), 4.15 (m, 1H), 5.97(br d, 1H), 7.2-7.4 (m, 6H), 8.04 (d, 1H), 10.11 (br s, 1H).

EXAMPLE 2

[0278] Step A: Preparation of 1-Ethyl-3-trifluoromethylpyrazol-5-ylCarboxylic Acid

[0279] To a mixture of 3-trifluoromethylpyrazole (5 g, 37 mmol) andpowdered potassium carbonate (10 g, 72 mmol) stirring in 30 mL ofN,N-dimethylformamide, iodoethane (8 g, 51 mmol) was added dropwise.After a mild exotherm, the reaction was stirred overnight at roomtemperature. The reaction mixture was partitioned between 100 mL ofdiethyl ether and 100 mL of water. The ether layer was separated, washedwith water (3×) and brine, and dried over magnesium sulfate. Evaporationof solvent in vacuo gave 4 g of oil.

[0280] To 3.8 g of this oil stirring in 40 mL of tetrahydrofuran undernitrogen in a dry ice/acetone bath, 17 mL of a 2.5 M solution of n-butyllithium in tetrahydrofuran (43 mmol) was added dropwise and the solutionstirred for 20 minutes at −78° C. An excess of gaseous carbon dioxidewas bubbled into the stirred solution at a moderate rate for 10 minutes.After addition of carbon dioxide, the reaction was allowed to slowlyreach room temperature and stirred overnight. The reaction mixture waspartitioned between diethyl ether (100 mL) and 0.5 N aqueous sodiumhydroxide (100 mL). The basic layer was separated and acidified withconcentrated hydrochloric acid to a pH of 2-3. The aqueous mixture wasextracted with ethyl acetate (100 mL) and the organic extract washedwith water and brine and dried over magnesium sulfate. The oily residue,which remained after evaporating the solvent in vacuo, was triturated toa solid from a small amount of n-butyl chloride. After filtering anddrying, a slightly impure, sample of1-ethyl-3-trifluoromethyl-pyrazol-5-yl carboxylic acid (1.4 g) wasobtained as a broad-melting solid.

[0281] 1H NMR (CDCl₃): 9.85 (br s,1H), 7.23 (s,1H), 4.68 (q,2H), 1.51(t,3H) ppm.

[0282] Step B: Preparation of 2-[1-Ethyl-3-trifluoromethylpyrazol-5-ylcarbamoyl]-3-methyl-N-(1-methylethyl)benzamide

[0283] To a solution of 1-ethyl-3-trifluoromethyl-pyrazol-5-ylcarboxylic acid (0.5 g, 2.4 mmol) stirring in 20 mL of methylenechloride, oxalyl chloride (1.2 mL, 14 mmol) was added. Upon addition of2 drops of N,N-dimethylformamide, foaming and bubbling occurred. Thereaction mixture was heated at reflux for 1 hr as a yellow solution.After cooling, the solvent was removed in vacuo and the resultingresidue dissolved in 20 mL of tetrahydrofuran. To the stirred solution,2-amino-3-methyl-N-(1-methylethyl)benzamide (0.7 g, 3.6 mmol) was addedfollowed by the dropwise addition of N,N-diisopropylethylamine (3 mL, 17mmol). After stirring at room temperature overnight, the reactionmixture was partitioned between ethyl acetate (100 mL) and 1N aqueoushydrochloric acid (75 mL). The separated organic layer was washed withwater and brine and dried over magnesium sulfate. Evaporating in vacuogave a white solid residue, which on purification by flash columnchromatography on silica gel (2:1 hexanes/ethyl acetate) afforded 0.5 gof the title compound, a compound of the present invention, melting at223-226° C.

[0284]¹H NMR (DMSO-D₆): 10.15 (s,1H), 8.05 (d,1H), 7.45 (s,1H),7.43-7.25 (m,3H), 4.58 (q,2H), 3.97 (m,1H), 2.45 (s,3H), 1.36 (t,3H),1.06 (d,6H) ppm.

EXAMPLE 3

[0285] Step A: Preparation ofS,S-dimethyl-N-[4-(trifluoromethyl)phenyl]sulfilimine

[0286] A solution of N-chlorosuccinimide (12-43 g, 93.1 mmol) in ˜170 mLof dichloromethane was added to a mixture of 4-(trifluoromethyl) aniline(15 g, 93.1 mmol) and dimethyl sulfide (6.35 g, 102 mmol) in 230 mL ofdichloromethane at −5-0° C. After the addition was complete, the mixturewas stirred at 0-5° C. for 1 h, and N-chlorosuccinimide (0.02 g, 4.64mmol) was added. After a further 30 minutes, the mixture was washed with500 mL of 1N sodium hydroxide.

[0287] The organic phase was dried and evaporated to give the product asa solid 19-72 g melting at 101-103° C. (after crystallization from ethylacetate/hexanes).

[0288] IR(Nujol) 1603, 1562, 1532, 1502, 1428, 1402, 1335, 1300, 1270,1185, 1150, 1103, 1067, 1000, 972, 940, 906, 837, 817 cm⁻¹.

[0289]¹H NMR (CDCl₃) δ 7.35 (d, J=8.8 Hz, 2 H), 6.84 (d, J=8.8 Hz, 2 H),2.67 (5, 3 H).

[0290] Step B: 2-[(methylthio)methyl]-4-(trifluoromethyl)benzenamine

[0291] Sodium methoxide in methanol (1.95 g, 9.02 mmol, 25%) was addedto S,S-dimethyl-N-[4-(trifluoromethyl)phenyl]sulfilimine from Step A (2g, 9.04 mmol) in 15 mL of toluene. The mixture was warmed to ˜80° C. for˜1 h. The mixture was allowed to cool to 25° C. and was poured into 100mL of water. The mixture was extracted with 2×100 mL of ethyl acetateand the combined extracts were dried and evaporated to give 1.8 g of theproduct as a solid melting at 65.5-67.5° C. (after crystallization fromhexanes).

[0292] IR(nujol) 3419, 3333, 1629, 1584, 1512, 1440, 1334, 1302, 1235,1193, 1139, 1098, 1078, 979, 904, 832 cm⁻¹.

[0293]¹ ¹H NMR (CDCl₃) δ 7.35 (dd, J=1.5 Hz×8.2 Hz, 1H) 6.72 (d, J=8.4Hz) 4.39 (br.5 2 H, 3.69 (5, 2 H), 1.99 (5, 3 H).

[0294] Step C: Preparation of 2-methyl-4-(trifluoromethyl)benzenamine

[0295] Activated Raney nickel (500 g wet paste, ˜50μ) was addedportionwise to a solution of2-[(methylthio)methyl]-4-(trifluoromethyl)benzenamine (55.3 g, 0.25mole) in 1 L of ethanol over 30 minutes at 25-30° C. The heterogeneousmixture was stirred vigorously for 30 minutes after the addition. Thestirring was stopped, and the solids were allowed to settle over onehour. The liquid was decanted from the solids and poured through filterpaper. The filtrate was evaporated under reduced pressure, and theresidue was taken up in dichloromethane. The organic phase was separatedfrom a small volume of water, dried over magnesium sulfate andevaporated under reduced pressure to afford 37.6 g of the title compoundas amber oil.

[0296]¹H NMR (CDCl₃) 67 7.28 (m,2H), 6.68 (d,1H), 3.87 (br s,2H), 2.19(s,3H).

[0297] Step D: Preparation of 2-methyl (trifluoromethyl)benzonitrile

[0298] Concentrated hydrochloric acid (16 mL) was added dropwise at amoderate rate to a heterogeneous mixture of2-methyl-4-(trifluoromethyl)benzenamine (14 g, 80 mmol) and 120 mL ofwater while stirring vigorously. A thick suspension resulted which wasstirred for 20 minutes, diluted with 280 mL of water and cooled to 5° C.A solution of sodium nitrite (5.5 g, 80 mmol) and 25 mL of water wasadded slowly to the reaction suspension. After stirring for 30 minutesat 5° C. a solution resulted which was stirred cold for 30 more minutesand then neutralized with potassium carbonate. This diazonium saltsolution was then added portionwise via cannula to a stirred, 95° C.mixture of potassium cyanide (22 g, 0.34 mole), copper sulfatepentahydrate (20 g, 80 mmol) and 140 mL of water. After the addition themixture was stirred for 30 minutes at 95° C. and then allowed to cool toroom temperature. Ether was added and the heterogeneous mixture wasfiltered through celite. The solids were washed with ether, and thefiltrate was partitioned. The aqueous phase was extracted with ether,and the combined organic extracts were dried over magnesium sulfate andconcentrated under reduced pressure to afford 13.1 g of the titlecompound as brown oil.

[0299]¹H NMR (CDCl₃) δ 7.74 (d,1H), 7.60 (s,1H), 7.55 (d,1H), 2.64(s,3H).

[0300] Step E: Preparation of 2-methyl-4-trifluoromethyl benzoic Acid

[0301] Potassium hydroxide (15.7 g, 0.28 mole) and 15 mL of water wereadded as a solution to a stirred, heterogeneous mixture of2-methyl-4-(trifluoromethyl)benzonitrile (13 g, 70 mmol) and 135 mL ofethylene glycol. The reaction mixture was heated at 120-130° C. for 20hours and allowed to cool to room temperature. The dark solution waspoured into 800 mL of water and filtered through celite. The filtratewas washed with ether and then the aqueous was acidified withconcentrated hydrochloric acid. This aqueous phase was extracted threetimes with ethyl acetate, the organic extracts were combined, dried overmagnesium sulfate and evaporated under reduced pressure to afford thetitle compound as a tan solid.

[0302]¹H NMR (CDCl₃) 67 7.98 (d,1H), 7.70 (s,1H), 7.65 (d,1H), 2.60(s,3H).

[0303] Step F: Preparation of 2-methyl-4-(trifluoromethoxy)benzoylchloride

[0304] Thionyl chloride (0.42 g, 3.5 mmol) was added to a solution ofthe benzoic acid from Step E (0.50 g, 2.4 mmol) in 10 mL of toluene atroom temperature. The reaction was refluxed for three hours then cooledto room temperature. The solvent was evaporated under reduced pressureand excess thionyl chloride was removed by azeotroping with toluene. Thebenzoyl chloride obtained was used directly in Step G.

[0305] Step G: Preparation of2-methyl-N-[2-methyl-6-[[(1-methylethyl)amino]-carbonyl]phenyl]-4-(trifluoromethyl)benzamide

[0306] The benzoyl chloride of Step F (0.29 g, 1.3 mmol) was added to amixture of the aniline from Example 1, Step B (0.36 g, 1.9 mmol) anddiisopropylethylamine (0.26 g, 2.0 mmol) in 10 mL of chloroform at roomtemperature. The reaction was allowed to stir overnight. The solidprecipitate was filtered and dried to afford 0.38 g of the titlecompound, a compound of the present invention, as a solid melting at247-248° C.

[0307]¹H NMR (CDCl₃) α 1.24 (d,6H), 2.41 (s,3H), 2.58 (s,3H), 4.20(m,1H), 5.94 (br d,1H), 7.2-7.3 (m,2H), 7.40 (d,1H), 7.52 (s,1H), 7.53(d,1H), 7.70 (d,1H), 9.36 (br s,1H).

EXAMPLE 4

[0308] Step A: Preparation of2-Methyl-6-(trifluoromethyl)-3-pyridinecarbonyl chloride

[0309] Thionyl chloride (4.35 g, 36.5 mmol) was added to a mixture of2-methyl-6-trifluoromethyl nicotinic acid (5.00 g, 24.4 mmol) in 75 mLof toluene and the mixture was heated at reflux for 3 hours. Thereaction was cooled to room temperature and the solvent was removedunder reduced pressure. Excess thionyl chloride was removed by azeotropewith toluene. The resultant acid chloride was used as is in Example 4,Step B.

[0310] Step B: Preparation of8-Methyl-2-[2-methyl-6-(trifluoromethyl)-3-pyridinyl]-4H-3,1-benzoxazine

[0311] A mixture of the 6-methyl isatoic anhydride (3.92 g, 22.1 mmol)and the acid chloride from Step A (5.45 g, 24.3 mmol) was heated atreflux in pyridine for 16 hours. The dark brown solution was cooled toroom temperature and the solvent was removed under reduced pressure.Excess pyridine was removed by azeotrope with toluene. Ether was addedand the resulting brown solid was removed by filtration. The solid wastaken up in a mixture of aqueous sodium bicarbonate and chloroform, thechloroform extracts were dried over magnesium sulfate and evaporated.Excess pyridine was again removed by azeotrope with toluene to afford5.1 g of the title compound as a brown solid.

[0312]¹H NMR (CDCl₃) d 2.65 (s,3H), 3.11 (s,3H), 7.49 (t,1H) 7.40(m,1H), 7.68-7.73 (m,2H), 1.11 (d,1H), 8.58 (d,1H).

[0313] Step C: Preparation of2-Methyl-N-[2-methyl-6-[[(1-methylethyl)amino]carbonyl]phenyl]-6-(trifluoromethyl)-3-pyridine

[0314] Isopropylamine (7.37 g, 0.125 mmol) was added to a mixture of thebenzoxazinone of Step B (4.00 g, 12.5 mmol) in 30 mL of tetrahydrofuran.A homogeneous solution formed. The mixture was heated briefly afterwhich a thick white precipitate formed. The solvent was removed underreduced pressure and the resultant solid was washed with ether andfiltered to afford 4.48 g of the title compound as a solid melting at247-248° C.

[0315]¹H NMR (CDCl₃) d 1.24 (d,6H), 2.41 (s,3H), 2.77 (s,3H), 4.17(m,1H), 5.96 (b,d,1H), 7.21 (m,2H) 7.40 (m,1H), 7.53 (d,1H), 7.97(d,1H), 9.80 (bs,1H).

EXAMPLE 5

[0316] Step A: Preparation of4-Methyl-N-[2-methyl-6-[[(1-methylethyl)amino]carbonyl]phenyl]-2-(trifluoromethyl)-5-primidinecarboxamide

[0317] To a solution 0.8 g (4 mmol) of4-methyl-2-tritluoromethylpyrimidine-5-carboxylic acid [made by themethod of Palanki et al, J. Med. Chem. 2000, 43, 3995] stirring in 15 mLof methylene chloride, oxalyl chloride (2 mL, 23 mmol) was added. Uponaddition of 2 drops of N,N-dimethylformamide, foaming and bubblingoccurred. The reaction mixture was heated at reflux for 1 hr as a yellowsolution. After cooling, the solvent was removed in vacuo and theresulting residue dissolved in 20 mL of tetrahydrofuran. To the stirredsolution, 2-amino-3-methyl-N-(1-methylethyl)benzamide (1 g, 5 mmol) wasadded followed by the dropwise addition of N,N-diisopropylethylamine (3ml, 17 mmol). After stirring at room temperature overnight, the reactionmixture was partitioned between ethyl acetate (200 mL) and 1N aqueoushydrochloric acid (75 mL). The separated organic layer was washed withwater and brine and dried over magnesium sulfate. Evaporating in vacuogave a white solid, which was suspended in a small amount of ethylacetate and filtered to afford (after drying) 650 mg of the titlecompound, a compound of the present invention, melting at 248-251° C.

[0318]¹H NMR (DMSO-D₆): 10.3 (s,NH), 9.07 (s,1H), 8.25 (d,NH), 7.43-7.25(m,3H), 4.03 (m,1H), 2.73 (s,3H), 2.32 (s,3H), 1.12 (d,6H) ppm.

EXAMPLE 6

[0319] Step A: Preparation of2-Methyl-1-phenyl-4-(trifuoromethyl)-1H-pyrazole

[0320] A solution of 1,1,1-trifluoropentane-2,4-dione (20.0 g, 0.130mole) in glacial acetic acid (60 mL) was cooled to 7° C. using anice/water bath. Phenylhydrazine (14.1 g, 0.130 mole) was added dropwiseover a period of 60 minutes. The reaction mass temperature increased to15° C. during the addition. The resulting orange solution was held underambient conditions for 60 minutes. The bulk of the acetic acid wasremoved by stripping on a rotary evaporator at a bath temperature of 65°C. The residue was dissolved in methylene chloride (150 mL). Thesolution was washed with aqueous sodium bicarbonate (3 g in 50 mLwater). The purple-red organic layer was separated, treated withactivated charcoal (2 g) and MgSO₄, then filtered. Volatiles wereremoved on a rotary evaporator. The crude product consisted of 28.0 g ofa rose-colored oil, which contained ˜89% the desired product and 11%1-phenyl-5-(trifluoromethyl)-3-methylpyrazole.

[0321]¹H NMR (DMSO-D₆) 67 2.35 (s,3H), 6.76 (s,1H), 7.6-7.5 (m,5H).

[0322] Step B: Preparation of1-Phenyl-3-(trifluoromethyl)-1H-pyrazole-5-carboxylic acid

[0323] A sample of crude 1-phenyl-3-(trifiuoromethyl)-5-methylpyrazole(˜89%, 50.0 g, 0.221 mole) was mixed with water (400 mL) and cetyltrimethylammonium chloride (4.00 g, 0.011 mole). The mixture was heatedto 95° C. Potassium permanganate was added in 10 equal portions, spacedat ˜8 minute intervals. The reaction mass was maintained at 95-100° C.during this period. After the last portion was added, the mixture washeld for ˜15 minutes at 95-100° C., whereupon the purple, permanganatecolor had been discharged. The reaction mass was filtered while hot(˜75° C.) through a 1 cm thick bed of Celite® on a 150 ml, coarse, glassfrit. The filter cake was washed with warm (˜50° C.) water (3×100 mL).The combined filtrate and washings were extracted with ether (2×100 mL)to remove a small amount of yellow, water-insoluble material. Theaqueous layer was purged with nitrogen to remove residual ether. Theclear, colorless alkaline solution was acidified by adding concentratedhydrochloric acid dropwise until the pH reached ˜1.3 (28 g, 0.28 mole).Gas evolution was vigorous during the first two-thirds of the addition.The product was collected via filtration, washed with water (3×40 mL),then dried overnight at 55° C. in vacuo. The product consisted of 11.7 gof a white, crystalline powder, which was essentially pure based upon ¹HNMR.

[0324]¹H NMR (CDCl₃) 67 7.33 (s,1H), 7.4-7.5 (m,5H).

[0325] Step C: Preparation of1-Phenyl-3-(trifluoromethyl)-1H-pyrazole-5-carbonyl chloride

[0326] A sample of crude1-phenyl-3-(trifluoromethyl)pyrazole-5-carboxylic acid (4.13 g, 16.1mmol) was dissolved in methylene chloride (45 mL). The solution wastreated with oxalyl chloride (1.80 mL, 20.6 mmol), followed byN,N-dimethylformamide (0.010 mL, 0.13 mmol). Off-gassing began shortlyafter adding the N,N-dimethylformamide catalyst. The reaction mixturewas stirred for ˜20 minutes under ambient conditions, then was heated toreflux for a period of 35 minutes. Volatiles were removed by strippingthe reaction mixture on a rotary evaporator at a bath temperature of 55°C. The product consisted of 4.43 g of a light-yellow oil. The onlyimpurity observed by ¹H NMR was N,N-dimethylformamide.

[0327]¹H NMR (CDCl₃) 67 7.40 (m,1H), 7.42 (s,1H), 7.50-7.53 (m,4H).

[0328] Step D: Preparation ofN-[2-Methyl-6-[[(1-methylethyl)amino]carbonyl]phenyl]-1-phenyl-3-(trifluoromethyl)-1H-pyrazole-5-carboxamide

[0329] A sample of 3-methylisatoic anhydride (0.30 g, 1.7 mmol)partially dissolved in pyridine (4.0 mL) was treated with1-phenyl-3-(trifluoromethylpyrazole)-5-carboxyl chloride (0.55 g, 1.9mmol). The mixture was heated to ˜95° C. for a period of 2 hours. Theresulting orange solution was cooled to 29° C., then was treated withisopropylamine (1.00 g, 16.9 mmol). The reaction mass self-heated to 39°C. It was further heated to 55° C. for a period of 30 minutes, whereuponmuch precipitate formed. The reaction mass was dissolved in methylenechloride (150 mL). The solution was washed with aqueous acid (5 mL conc.HCl in 45 mL water), then with aqueous base (2 g sodium carbonate in 50mL water). The organic layer was dried over MgSO₄, filtered, thenconcentrated on a rotary evaporator. Upon reduction to ˜4 mL, productcrystals had formed. The slurry was diluted with ˜10 mL of ether,whereupon more product precipitated. The product was isolated byfiltration, washed with ether (2×10 mL), then washed with water (2×50mL). The wet cake was dried for 30 minutes at 70° C. in vacuo. Theproduct consisted of 0.52 g of an off-white powder melting at 260-262°C.

[0330]¹H NMR (DMSO-D₆) δ 1.07 (d,6H), 2.21 (s,3H), 4.02 (octet,1H),7.2-7.4 (m,3H), 7.45-7.6 (m,6H), 8.10 (d,1H), 10.31 (s,1H).

EXAMPLE 7

[0331] Step A: Preparation of3-Trifluoromethyl-2-[3-(trifluoromethyl)-1H-pyrazol-1-yl]pyridine

[0332] A mixture of 2-chloro-3-trifluoromethylpyridine (3.62 g., 21mmol), 3-trifiluoromethylpyrazole (2.7 g., 20 mmol ), and potassiumcarbonate (6.0 g., 43 mmol ) were heated at 100° C. for 18 h. The cooledreaction mixture was added to ice/water (100 mL). The mixture wasextracted twice with ether (100 mL) and the combined ether extracts werewashed twice with water (100 mL). The organic layer was dried withmagnesium sulfate and concentrated to an oil. Chromatography on silicagel with hexanes:ethyl acetate 8:1 to 4:1 as eluent gave the titlecompound (3.5 g) as an oil. ¹H NMR (CDCl₃) δ 6.75 (m,1H), 7.5 (m,1H),8.2 (m,2H), 8.7 (m,1H).

[0333] Step B: Preparation of3-(Trifluoromethyl)-1-[3-(trifluoromethyl)-2-pyridinyl]-1H-pyrazole-5-carboxylicacid

[0334] A mixture of the title compound of Example 5, Step A (3.4 g, 13mmol) was dissolved in tetrahydrofuran (30 mL) and cooled to −70° C.Lithium diisopropylamide (2N in heptane/tetrahydrofuran, (Aldrich) 9.5mL, 19 mmol) was added and the resulting dark mixture was stirred for 10minutes. Dry carbon dioxide was bubbled through the mixture for 15minutes. The mixture was allowed to warm to 23° C. and treated withwater (50 mL) and 1 N sodium hydroxide (10 mL). The aqueous mixture wasextracted with ether (100 mL) and then ethyl acetate (100 mL). Theaqueous layer was acidified with 6N hydrochloric acid to pH 1-2 andextracted twice with dichloromethane. The organic layer was dried withmagnesium sulfate and concentrated to give the title compound (1.5 g).¹H NMR (CDCl₃) δ 7.6 (m,1H), 7.95 (m,1H), 8.56 (m,1H)), 8.9 (m,1H), 14.2(br,1H)

[0335] Step C: Preparation ofN-[2-Methyl-6-[[(1-methylethyl)amino]carbonyl]phenyl]-3-(trifluoromethyl)-1-[3-(trifluoromethyl)-2-pyridinyl]-1-1H-pyrazole-5-carboxamide

[0336] A mixture of the title compound of Example 5, Step B (0.54 g, 1.1mmol), the title compound from Example 1, Step B (0.44 g, 2.4 mmol) andbop chloride (bis(2-oxo-oxazolidinyl)phosphinyl chloride, 0.54 g, 2.1mmol) in acetonitrile (13 mL) was treated with triethylamine (0.9 mL).The mixture was shaken in a closed scintillation vial for 18 h. Thereaction was partitioned between ethyl acetate (100 mL) and 1Nhydrochloric acid. The ethyl acetate layer was washed successively with1N hydrochloric acid (50 mL), 1N sodium hydroxide (50 mL) and saturatedsodium chloride solution (50 mL). The organic layer was dried overmagnesium sulfate and concentrated. The residue was subjected to columnchromatography on silica gel with hexanes/ethyl acetate (5:1 to 3:1) aseluent. The title compound (0.43 g) was isolated as a white solid. m.p.227-230° C. ¹H NMR (CDCl₃) δ 1.2 (m, 6H), 4.15 (m, 1H), 5.9 (br d,1H),7.1 (m,1H), 7.2 (m,2H), 7.4 (s,1H), 7.6 (m,1H), 8.15 (m,1H), 8.74(m,1H), 10.4 (br,1H).

[0337] By the procedures described herein together with methods known inthe art, the following compounds of Tables 1 to 17 can be prepared. Thefollowing abbreviations are used in the Tables: t is tertiary, s issecondary, n is normal, i is iso, c is cyclo, Me is methyl, Et is ethyl,Pr is propyl, i-Pr is isopropyl, t-Bu is tert butyl, Ph is phenyl, OMeis methoxy, OEt is ethoxy, SMe is methylthio, SEt is ethylthio, CN iscyano, NO₂ is nitro, TMS is trimethylsilyl, S(O)Me is methylsulfinyl,and S(O)₂Me is methylsulfonyl. TABLE 1

R⁴ R⁵ and/or R⁶ Me 2-CF₃ Me 2-OCF₃ Me 2-OCF₂H Me 2-OCF₂CF₂H Me 2-OCH₂CF₃Me 2-SCF₃ Me 2-SOCF₃ Me 2-SO₂CF₃ Me 2-SCF₂H Me 2-SOCF₂H Me 2-SO₂CF₂H Cl2-CF₃ Cl 2-OCF₃ Cl 2-OCF₂H Cl 2-OCF₂CF₂H Cl 2-OCH₂CF₃ Cl 2-SCF₃ Cl2-SOCF₃ Cl 2-SO₂CF₃ Cl 2-SCF₂H Cl 2-SOCF₂H Cl 2-SO₂CF₂H F 2-CF₃ F 2-OCF₃F 2-OCF₂H F 2-OCF₂CF₂H F 2-OCH₂CF₃ F 2-SCF₃ F 2-SOCF₃ F 2-SO₂CF₃ F2-SCF₂H F 2-SOCF₂H F 2-SO₂CF₂H Br 2-CF₃ Br 2-OCF₃ Br 2-OCF₂H Br2-OCF₂CF₂H Br 2-OCH₂CF₃ Br 2-SCF₃ Br 2-SOCF₃ Br 2-SO₂CF₃ Br 2-SCF₂H Br2-SOCF₂H Br 2-SO₂CF₂H I 2-CF₃ I 2-OCF₃ I 2-OCF₂H I 2-OCF₂CF₂H I2-OCH₂CF₃ I 2-SCF₃ I 2-SOCF₃ I 2-SO₂CF₃ I 2-SCF₂H I 2-SOCF₂H I 2-SO₂CF₂HOMe 2-CF₃ OMe 2-OCF₃ OMe 2-OCF₂H OMe 2-OCF₂CF₂H OMe 2-OCH₂CF₃ OMe 2-SCF₃OMe 2-SOCF₃ OMe 2-SO₂CF₃ OMe 2-SCF₂H OMe 2-SOCF₂H OMe 2-SO₂CF₂H CF₃2-CF₃ CF₃ 2-OCF₃ CF₃ 2-OCF₂H CF₃ 2-OCF₂CF₂H CF₃ 2-OCH₂CF₃ CF₃ 2-SCF₃ CF₃2-SOCF₃ CF₃ 2-SO₂CF₃ CF₃ 2-SCF₂H CF₃ 2-SOCF₂H CF₃ 2-SO₂CF₂H OCF₂H 2-CF₃OCF₂H 2-OCF₃ OCF₂H 2-OCF₂H OCF₂H 2-OCF₂CF₂H OCF₂H 2-OCH₂CF₃ OCF₂H 2-SCF₃OCF₂H 2-SOCF₃ OCF₂H 2-SO₂CF₃ OCF₂H 2-SCF₂H OCF₂H 2-SOCF₂H OCF₂H2-SO₂CF₂H Me 2-Me-4-CF₃ Me 2-Me-4-OCF₃ Me 2-Me-4-OCF₂H Me 2-Me-4-OCH₂CF₃Me 2-Me-4-SCF₃ Me 2-Me-4-SOCF₃ Me 2-Me-4-SO₂CF₃ Me 2-Me-4-SCF₂H Me2-Me-4-SOCF₂H Me 2-Me-4-SO₂CF₂H Br 2-Me-4-CF₃ Br 2-Me-4-OCF₃ Br2-Me-4-OCF₂H Br 2-Me-4-OCH₂CF₃ Br 2-Me-4-SCF₃ Br 2-Me-4-SOCF₃ Br2-Me-4-SO₂CF₃ Br 2-Me-4-SCF₂H Br 2-Me-4-SOCF₂H Br 2-Me-4-SO₂CF₂H CF₃2-Me-4-CF₃ CF₃ 2-Me-4-OCF₃ CF₃ 2-Me-4-OCF₂H CF₃ 2-Me-4-OCH₂CF₃ CF₃2-Me-4-SCF₃ CF₃ 2-Me-4-SOCF₃ CF₃ 2-Me-4-SO₂CF₃ CF₃ 2-Me-4-SCF₂H CF₃2-Me-4-SOCF₂H CF₃ 2-Me-4-SO₂CF₂H Me 3-CF₃ Me 3-OCF₃ Me 3-OCF₂H Me3-OCF₂CF₂H Me 3-OCH₂CF₃ Me 3-SCF₃ Me 3-SOCF₃ Me 3-SO₂CF₃ Me 3-SCF₂H Me3-SOCF₂H Me 3-SO₂CF₂H Cl 3-CF₃ Cl 3-OCF₃ Cl 3-OCF₂H Cl 3-OCF₂CF₂H Cl3-OCH₂CF₃ Cl 3-SCF₃ Cl 3-SOCF₃ Cl 3-SO₂CF₃ Cl 3-SCF₂H Cl 3-SOCF₂H Cl3-SO₂CF₂H F 3-CF₃ F 3-OCF₃ F 3-OCF₂H F 3-OCF₂CF₂H F 3-OCH₂CF₃ F 3-SCF₃ F3-SOCF₃ F 3-SO₂CF₃ F 3-SCF₂H F 3-SOCF₂H F 3-SO₂CF₂H Br 3-CF₃ Br 3-OCF₃Br 3-OCF₂H Br 3-OCF₂CF₂H Br 3-OCH₂CF₃ Br 3-SCF₃ Br 3-SOCF₃ Br 3-SO₂CF₃Br 3-SCF₂H Br 3-SOCF₂H Br 3-SO₂CF₂H I 3-CF₃ I 3-OCF₃ I 3-OCF₂H I3-OCF₂CF₂H I 3-OCH₂CF₃ I 3-SCF₃ I 3-SOCF₃ I 3-SO₂CF₃ I 3-SCF₂H I3-SOCF₂H I 3-SO₂CF₂H OMe 3-CF₃ OMe 3-OCF₃ OMe 3-OCF₂H OMe 3-OCF₂CF₂H OMe3-OCH₂CF₃ OMe 3-SCF₃ OMe 3-SOCF₃ OMe 3-SO₂CF₃ OMe 3-SCF₂H OMe 3-SOCF₂HOMe 3-SO₂CF₂H CF₃ 3-CF₃ CF₃ 3-OCF₃ CF₃ 3-OCF₂H CF₃ 3-OCF₂CF₂H CF₃3-OCH₂CF₃ CF₃ 3-SCF₃ CF₃ 3-SOCF₃ CF₃ 3-SO₂CF₃ CF₃ 3-SCF₂H CF₃ 3-SOCF₂HCF₃ 3-SO₂CF₂H OCF₂H 3-CF₃ OCF₂H 3-OCF₃ OCF₂H 3-OCF₂H OCF₂H 3-OCF₂CF₂HOCF₂H 3-OCH₂CF₃ OCF₂H 3-SCF₃ OCF₂H 3-SOCF₃ OCF₂H 3-SO₂CF₃ OCF₂H 3-SCF₂HOCF₂H 3-SOCF₂H OCF₂H 3-SO₂CF₂H F 2-Me-4-CF₃ F 2-Me-4-OCF₃ F 2-Me-4-OCF₂HF 2-Me-4-OCH₂CF₃ F 2-Me-4-SCF₃ F 2-Me-4-SOCF₃ F 2-Me-4-SO₂CF₃ F2-Me-4-SCF₂H F 2-Me-4-SOCF₂H F 2-Me-4-SO₂CF₂H I 2-Me-4-CF₃ I 2-Me-4-OCF₃I 2-Me-4-OCF₂H I 2-Me-4-OCH₂CF₃ I 2-Me-4-SCF₃ I 2-Me-4-SOCF₃ I2-Me-4-SO₂CF₃ I 2-Me-4-SCF₂H I 2-Me-4-SOCF₂H I 2-Me-4-SO₂CF₂H NO₂2-Me-4-CF₃ NO₂ 2-Me-4-OCF₃ NO₂ 2-Me-4-OCF₂H NO₂ 2-Me-4-OCH₂CF₃ NO₂2-Me-4-SCF₃ NO₂ 2-Me-4-SOCF₃ NO₂ 2-Me-4-SO₂CF₃ NO₂ 2-Me-4-SCF₂H NO₂2-Me-4-SOCF₂H NO₂ 2-Me-4-SO₂CF₂H Me 4-CF₃ Me 4-OCF₃ Me 4-OCF₂H Me4-OCF₂CF₂H Me 4-OCH₂CF₃ Me 4-SCF₃ Me 4-SOCF₃ Me 4-SO₂CF₃ Me 4-SCF₂H Me4-SOCF₂H Me 4-SO₂CF₂H Cl 4-CF₃ Cl 4-OCF₃ Cl 4-OCF₂H Cl 4-OCF₂CF₂H Cl4-OCH₂CF₃ Cl 4-SCF₃ Cl 4-SOCF₃ Cl 4-SO₂CF₃ Cl 4-SCF₂H Cl 4-SOCF₂H Cl4-SO₂CF₂H F 4-CF₃ F 4-OCF₃ F 4-OCF₂H F 4-OCF₂CF₂H F 4-OCH₂CF₃ F 4-SCF₃ F4-SOCF₃ F 4-SO₂CF₃ F 4-SCF₂H F 4-SOCF₂H F 4-SO₂CF₂H Br 4-CF₃ Br 4-OCF₃Br 4-OCF₂H Br 4-OCF₂CF₂H Br 4-OCH₂CF₃ Br 4-SCF₃ Br 4-SOCF₃ Br 4-SO₂CF₃Br 4-SCF₂H Br 4-SOCF₂H Br 4-SO₂CF₂H I 4-CF₃ I 4-OCF₃ I 4-OCF₂H I4-OCF₂CF₂H I 4-OCH₂CF₃ I 4-SCF₃ I 4-SOCF₃ I 4-SO₂CF₃ I 4-SCF₂H I4-SOCF₂H I 4-SO₂CF₂H OMe 4-CF₃ OMe 4-OCF₃ OMe 4-OCF₂H OMe 4-OCF₂CF₂H OMe4-OCH₂CF₃ OMe 4-SCF₃ OMe 4-SOCF₃ OMe 4-SO₂CF₃ OMe 4-SCF₂H OMe 4-SOCF₂HOMe 4-SO₂CF₂H CF₃ 4-CF₃ CF₃ 4-OCF₃ CF₃ 4-OCF₂H CF₃ 4-OCF₂CF₂H CF₃4-OCH₂CF₃ CF₃ 4-SCF₃ CF₃ 4-SOCF₃ CF₃ 4-SO₂CF₃ CF₃ 4-SCF₂H CF₃ 4-SOCF₂HCF₃ 4-SO₂CF₂H OCF₂H 4-CF₃ OCF₂H 4-OCF₃ OCF₂H 4-OCF₂H OCF₂H 4-OCF₂CF₂HOCF₂H 4-OCH₂CF₃ OCF₂H 4-SCF₃ OCF₂H 4-SOCF₃ OCF₂H 4-SO₂CF₃ OCF₂H 4-SCF₂HOCF₂H 4-SOCF₂H OCF₂H 4-SO₂CF₂H Cl 2-Me-4-CF₃ Cl 2-Me-4-OCF₃ Cl2-Me-4-OCF₂H Cl 2-Me-4-OCH₂CF₃ Cl 2-Me-4-SCF₃ Cl 2-Me-4-SOCF₃ Cl2-Me-4-SO₂CF₃ Cl 2-Me-4-SCF₂H Cl 2-Me-4-SOCF₂H Cl 2-Me-4-SO₂CF₂H OMe2-Me-4-CF₃ OMe 2-Me-4-OCF₃ OMe 2-Me-4-OCF₂H OMe 2-Me-4-OCH₂CF₃ OMe2-Me-4-SCF₃ OMe 2-Me-4-SOCF₃ OMe 2-Me-4-SO₂CF₃ OMe 2-Me-4-SCF₂H OMe2-Me-4-SOCF₂H OMe 2-Me-4-SO₂CF₂H SMe 2-Me-4-CF₃ SMe 2-Me-4-OCF₃ SMe2-Me-4-OCF₂H SMe 2-Me-4-OCH₂CF₃ SMe 2-Me-4-SCF₃ SMe 2-Me-4-SOCF₃ SMe2-Me-4-SO₂CF₃ SMe 2-Me-4-SCF₂H SMe 2-Me-4-SOCF₂H SMe 2-Me-4-SO₂CF₂H

[0338] TABLE 2

R⁴ R⁵ and/or R⁶ Me 2-CF₃ Me 2-OCF₃ Me 2-OCF₂H Me 2-OCF₂CF₂H Me 2-OCH₂CF₃Me 2-SCF₃ Me 2-SOCF₃ Me 2-SO₂CF₃ Me 2-SCF₂H Me 2-SOCF₂H Me 2-SO₂CF₂H Cl2-CF₃ Cl 2-OCF₃ Cl 2-OCF₂H Cl 2-OCF₂CF₂H Cl 2-OCH₂CF₃ Cl 2-SCF₃ Cl2-SOCF₃ Cl 2-SO₂CF₃ Cl 2-SCF₂H Cl 2-SOCF₂H Cl 2-SO₂CF₂H F 2-CF₃ F 2-OCF₃F 2-OCF₂H F 2-OCF₂CF₂H F 2-OCH₂CF₃ F 2-SCF₃ F 2-SOCF₃ F 2-SO₂CF₃ F2-SCF₂H F 2-SOCF₂H F 2-SO₂CF₂H Br 2-CF₃ Br 2-OCF₃ Br 2-OCF₂H Br2-OCF₂CF₂H Br 2-OCH₂CF₃ Br 2-SCF₃ Br 2-SOCF₃ Br 2-SO₂CF₃ Br 2-SCF₂H Br2-SOCF₂H Br 2-SO₂CF₂H I 2-CF₃ I 2-OCF₃ I 2-OCF₂H I 2-OCF₂CF₂H I2-OCH₂CF₃ I 2-SCF₃ I 2-SOCF₃ I 2-SO₂CF₃ I 2-SCF₂H I 2-SOCF₂H I 2-SO₂CF₂HOMe 2-CF₃ OMe 2-OCF₃ OMe 2-OCF₂H OMe 2-OCF₂CF₂H OMe 2-OCH₂CF₃ OMe 2-SCF₃OMe 2-SOCF₃ OMe 2-SO₂CF₃ OMe 2-SCF₂H OMe 2-SOCF₂H OMe 2-SO₂CF₂H CF₃2-CF₃ CF₃ 2-OCF CF₃ 2-OCF₂H CF₃ 2-OCF₂CF₂H CF₃ 2-OCH₂CF₃ CF₃ 2-SCF₃ CF₃2-SOCF₃ CF₃ 2-SO₂CF₃ CF₃ 2-SCF₂H CF₃ 2-SOCF₂H CF₃ 2-SO₂CF₂H OCF₂H 2-CF₃OCF₂H 2-OCF₃ OCF₂H 2-OCF₂H OCF₂H 2-OCF₂CF₂H OCF₂H 2-OCH₂CF₃ OCF₂H 2-SCF₃OCF₂H 2-SOCF₃ OCF₂H 2-SO₂CF₃ OCF₂H 2-SCF₂H OCF₂H 2-SOCF₂H OCF₂H2-SO₂CF₂H Me 2-Me-4-CF₃ Me 2-Me-4-OCF₃ Me 2-Me-4-OCF₂H Me 2-Me-4-OCH₂CF₃Me 2-Me-4-SCF₃ Me 2-Me-4-SOCF₃ Me 2-Me-4-SO₂CF₃ Me 2-Me-4-SCF₂H Me2-Me-4-SOCF₂H Me 2-Me-4-SO₂CF₂H Br 2-Me-4-CF₃ Br 2-Me-4-OCF₃ Br2-Me-4-OCF₂H Br 2-Me-4-OCH₂CF₃ Br 2-Me-4-SCF₃ Br 2-Me-4-SOCF₃ Br2-Me-4-SO₂CF₃ Br 2-Me-4-SCF₂H Br 2-Me-4-SOCF₂H Br 2-Me-4-SO₂CF₂H CF₃2-Me-4-CF₃ CF₃ 2-Me-4-OCF₃ CF₃ 2-Me-4-OCF₂H CF₃ 2-Me-4-OCH₂CF₃ CF₃2-Me-4-SCF₃ CF₃ 2-Me-4-SOCF₃ CF₃ 2-Me-4-SO₂CF₃ CF₃ 2-Me-4-SCF₂H CF₃2-Me-4-SOCF₂H CF₃ 2-Me-4-SO₂CF₂H Me 3-CF₃ Me 3-OCF₃ Me 3-OCF₂H Me3-OCF₂CF₂H Me 3-OCH₂CF₃ Me 3-SCF₃ Me 3-SOCF₃ Me 3-SO₂CF₃ Me 3-SCF₂H Me3-SOCF₂H Me 3-SO₂CF₂H Cl 3-CF₃ Cl 3-OCF₃ Cl 3-OCF₂H Cl 3-OCF₂CF₂H Cl3-OCH₂CF₃ Cl 3-SCF₃ Cl 3-SOCF₃ Cl 3-SO₂CF₃ Cl 3-SCF₂H Cl 3-SOCF₂H Cl3-SO₂CF₂H F 3-CF₃ F 3-OCF₃ F 3-OCF₂H F 3-OCF₂CF₂H F 3-OCH₂CF₃ F 3-SCF₃ F3-SOCF₃ F 3-SO₂CF₃ F 3-SCF₂H F 3-SOCF₂H F 3-SO₂CF₂H Br 3-CF₃ Br 3-OCF₃Br 3-OCF₂H Br 3-OCF₂CF₂H Br 3-OCH₂CF₃ Br 3-SCF₃ Br 3-SOCF₃ Br 3-SO₂CF₃Br 3-SCF₂H Br 3-SOCF₂H Br 3-SO₂CF₂H I 3-CF₃ I 3-OCF₃ I 3-OCF₂H I3-OCF₂CF₂H I 3-OCH₂CF₃ I 3-SCF₃ I 3-SOCF₃ I 3-SO₂CF₃ I 3-SCF₂H I3-SOCF₂H I 3-SO₂CF₂H OMe 3-CF₃ OMe 3-OCF₃ OMe 3-OCF₂H OMe 3-OCF₂CF₂H OMe3-OCH₂CF₃ OMe 3-SCF₃ OMe 3-SOCF₃ OMe 3-SO₂CF₃ OMe 3-SCF₂H OMe 3-SOCF₂HOMe 3-SO₂CF₂H CF₃ 3-CF₃ CF₃ 3-OCF₃ CF₃ 3-OCF₂H CF₃ 3-OCF₂CF₂H CF₃3-OCH₂CF₃ CF₃ 3-SCF₃ CF₃ 3-SOCF₃ CF₃ 3-SO₂CF₃ CF₃ 3-SCF₂H CF₃ 3-SOCF₂HCF₃ 3-SO₂CF₂H OCF₂H 3-CF₃ OCF₂H 3-OCF₃ OCF₂H 3-OCF₂H OCF₂H 3-OCF₂CF₂HOCF₂H 3-OCH₂CF₃ OCF₂H 3-SCF₃ OCF₂H 3-SOCF₃ OCF₂H 3-SO₂CF₃ OCF₂H 3-SCF₂HOCF₂H 3-SOCF₂H OCF₂H 3-SO₂CF₂H F 2-Me-4-CF₃ F 2-Me-4-OCF₃ F 2-Me-4-OCF₂HF 2-Me-4-OCH₂CF₃ F 2-Me-4-SCF₃ F 2-Me-4-SOCF₃ F 2-Me-4-SO₂CF₃ F2-Me-4-SCF₂H F 2-Me-4-SOCF₂H F 2-Me-4-SO₂CF₂H I 2-Me-4-Cl₃ I 2-Me-4-OCF₃I 2-Me-4-OCF₂H I 2-Me-4-OCH₂CF₃ I 2-Me-4-SCF₃ I 2-Me-4-SOCF₃ I2-Me-4-SO₂CF₃ I 2-Me-4-SCF₂H I 2-Me-4-SOCF₂H I 2-Me-4-SO₂CF₂H NO₂2-Me-4-CF₃ NO₂ 2-Me-4-OCF₃ NO₂ 2-Me-4-OCF₂H NO₂ 2-Me-4-OCH₂CF₃ NO₂2-Me-4-SCF₃ NO₂ 2-Me-4-SOCF₃ NO₂ 2-Me-4-SO₂CF₃ NO₂ 2-Me-4-SCF₂H NO₂2-Me-4-SOCF₂H NO₂ 2-Me-4-SO₂CF₂H Me 4-CF₃ Me 4-OCF₃ Me 4-OCF₂H Me4-OCF₂CF₂H Me 4-OCH₂CF₃ Me 4-SCF₃ Me 4-SOCF₃ Me 4-SO₂CF₃ Me 4-SCF₂H Me4-SOCF₂H Me 4-SO₂CF₂H Cl 4-CF₃ Cl 4-OCF₃ Cl 4-OCF₂H Cl 4-OCF₂CF₂H Cl4-OCH₂CF₃ Cl 4-SCF₃ Cl 4-SOCF₃ Cl 4-SO₂CF₃ Cl 4-SCF₂H Cl 4-SOCF₂H Cl4-SO₂CF₂H F 4-CF₃ F 4-OCF₃ F 4-OCF₂H F 4-OCF₂CF₂H F 4-OCH₂CF₃ F 4-SCF₃ F4-SOCF₃ F 4-SO₂CF₃ F 4-SCF₂H F 4-SOCF₂H F 4-SO₂CF₂H Br 4-CF₃ Br 4-OCF₃Br 4-OCF₂H Br 4-OCF₂CF₂H Br 4-OCH₂CF₃ Br 4-SCF₃ Br 4-SOCF₃ Br 4-SO₂CF₃Br 4-SCF₂H Br 4-SOCF₂H Br 4-SO₂CF₂H I 4-CF₃ I 4-OCF₃ I 4-OCF₂H I4-OCF₂CF₂H I 4-OCH₂CF₃ I 4-SCF₃ I 4-SOCF₃ I 4-SO₂CF₃ I 4-SCF₂H I4-SOCF₂H I 4-SO₂CF₂H OMe 4-CF₃ OMe 4-OCF₃ OMe 4-OCF₂H OMe 4-OCF₂CF₂H OMe4-OCH₂CF₃ OMe 4-SCF₃ OMe 4-SOCF₃ OMe 4-SO₂CF₃ OMe 4-SCF₂H OMe 4-SOCF₂HOMe 4-SO₂CF₂H CF₃ 4-CF₃ CF₃ 4-OCF₃ CF₃ 4-OCF₂H CF₃ 4-OCF₂CF₂H CF₃4-OCH₂CF₃ CF₃ 4-SCF₃ CF₃ 4-SOCF₃ CF₃ 4-SO₂CF₃ CF₃ 4-SCF₂H CF₃ 4-SOCF₂HCF₃ 4-SO₂CF₂H OCF₂H 4-CF₃ OCF₂H 4-OCF₃ OCF₂H 4-OCF₂H OCF₂H 4-OCF₂CF₂HOCF₂H 4-OCH₂CF₃ OCF₂H 4-SCF₃ OCF₂H 4-SOCF₃ OCF₂H 4-SO₂CF₃ OCF₂H 4-SCF₂HOCF₂H 4-SOCF₂H OCF₂H 4-SO₂CF₂H Cl 2-Me-4-CF₃ Cl 2-Me-4-OCF₃ Cl2-Me-4-OCF₂H Cl 2-Me-4-OCH₂CF₃ Cl 2-Me-4-SCF₃ Cl 2-Me-4-SOCF₃ Cl2-Me-4-SO₂CF₃ Cl 2-Me-4-SCF₂H Cl 2-Me-4-SOCF₂H Cl 2-Me-4-SO₂CF₂H OMe2-Me-4-CF₃ OMe 2-Me-4-OCF₃ OMe 2-Me-4-OCF₂H OMe 2-Me-4-OCH₂CF₃ OMe2-Me-4-SCF₃ OMe 2-Me-4-SOCF₃ OMe 2-Me-4-SO₂CF₃ OMe 2-Me-4-SCF₂H OMe2-Me-4-SOCF₂H OMe 2-Me-4-SO₂CF₂H SMe 2-Me-4-CF₃ SMe 2-Me-4-OCF₃ SMe2-Me-4-OCF₂H SMe 2-Me-4-OCH₂CF₃ SMe 2-Me-4-SCF₃ SMe 2-Me-4-SOCF₃ SMe2-Me-4-SO₂CF₃ SMe 2-Me-4-SCF₂H SMe 2-Me-4-SOCF₂H SMe 2-Me-4-SO₂CF₂H

[0339] TABLE 3

R⁴ R⁵ and/or R⁶ Me 2-CF₃ Me 2-OCF₃ Me 2-OCF₂H Me 2-OCF₂CF₂H Me 2-OCH₂CF₃Me 2-SCF₃ Me 2-SOCF₃ Me 2-SO₂CF₃ Me 2-SCF₂H Me 2-SOCF₂H Me 2-SO₂CF₂H Cl2-CF₃ Cl 2-OCF₃ Cl 2-OCF₂H Cl 2-OCF₂CF₂H Cl 2-OCH₂CF₃ Cl 2-SCF₃ Cl2-SOCF₃ Cl 2-SO₂CF₃ Cl 2-SCF₂H Cl 2-SOCF₂H Cl 2-SO₂CF₂H F 2-CF₃ F 2-OCF₃F 2-OCF₂H F 2-OCF₂CF₂H F 2-OCH₂CF₃ F 2-SCF₃ F 2-SOCF₃ F 2-SO₂CF₃ F2-SCF₂H F 2-SOCF₂H F 2-SO₂CF₂H Br 2-CF₃ Br 2-OCF₃ Br 2-OCF₂H Br2-OCF₂CF₂H Br 2-OCH₂CF₃ Br 2-SCF₃ Br 2-SOCF₃ Br 2-SO₂CF₃ Br 2-SCF₂H Br2-SOCF₂H Br 2-SO₂CF₂H I 2-CF₃ I 2-OCF₃ I 2-OCF₂H I 2-OCF₂CF₂H I2-OCH₂CF₃ I 2-SCF₃ I 2-SOCF₃ I 2-SO₂CF₃ I 2-SCF₂H I 2-SOCF₂H I 2-SO₂CF₂HOMe 2-CF₃ OMe 2-OCF₃ OMe 2-OCF₂H OMe 2-OCF₂CF₂H OMe 2-OCH₂CF₃ OMe 2-SCF₃OMe 2-SOCF₃ OMe 2-SO₂CF₃ OMe 2-SCF₂H OMe 2-SOCF₂H OMe 2-SO₂CF₂H CF₃2-CF₃ CF₃ 2-OCF₃ CF₃ 2-OCF₂H CF₃ 2-OCF₂CF₂H CF₃ 2-OCH₂CF₃ CF₃ 2-SCF₃ CF₃2-SOCF₃ CF₃ 2-SO₂CF₃ CF₃ 2-SCF₂H CF₃ 2-SOCF₂H CF₃ 2-SO₂CF₂H OCF₂H 2-CF₃OCF₂H 2-OCF₃ OCF₂H 2-OCF₂H OCF₂H 2-OCF₂CF₂H OCF₂H 2-OCH₂CF₃ OCF₂H 2-SCF₃OCF₂H 2-SOCF₃ OCF₂H 2-SO₂CF₃ OCF₂H 2-SCF₂H OCF₂H 2-SOCF₂H OCF₂H2-SO₂CF₂H Me 2-Me-4-CF₃ Me 2-Me-4-OCF₃ Me 2-Me-4-OCF₂H Me 2-Me-4-OCH₂CF₃Me 2-Me-4-SCF₃ Me 2-Me-4-SOCF₃ Me 2-Me-4-SO₂CF₃ Me 2-Me-4-SCF₂H Me2-Me-4-SOCF₂H Me 2-Me-4-SO₂CF₂H Br 2-Me-4-CF₃ Br 2-Me-4-OCF₃ Br2-Me-4-OCF₂H Br 2-Me-4-OCH₂CF₃ Br 2-Me-4-SCF₃ Br 2-Me-4-SOCF₃ Br2-Me-4-SO₂CF₃ Br 2-Me-4-SCF₂H Br 2-Me-4-SOCF₂H Br 2-Me-4-SO₂CF₂H CF₃2-Me-4-CF₃ CF₃ 2-Me-4-OCF₃ CF₃ 2-Me-4-OCF₂H CF₃ 2-Me-4-OCH₂CF₃ CF₃2-Me-4-SCF₃ CF₃ 2-Me-4-SOCF₃ CF₃ 2-Me-4-SO₂CF₃ CF₃ 2-Me-4-SCF₂H CF₃2-Me-4-SOCF₂H CF₃ 2-Me-4-SO₂CF₂H Me 3-CF₃ Me 3-OCF₃ Me 3-OCF₂H Me3-OCF₂CF₂H Me 3-OCH₂CF₃ Me 3-SCF₃ Me 3-SOCF₃ Me 3-SO₂CF₃ Me 3-SCF₂H Me3-SOCF₂H Me 3-SO₂CF₂H Cl 3-CF₃ Cl 3-OCF₃ Cl 3-OCF₂H Cl 3-OCF₂CF₂H Cl3-OCH₂CF₃ Cl 3-SCF₃ Cl 3-SOCF₃ Cl 3-SO₂CF₃ Cl 3-SCF₂H Cl 3-SOCF₂H Cl3-SO₂CF₂H F 3-CF₃ F 3-OCF₃ F 3-OCF₂H F 3-OCF₂CF₂H F 3-OCH₂CF₃ F 3-SCF₃ F3-SOCF₃ F 3-SO₂CF₃ F 3-SCF₂H F 3-SOCF₂H F 3-SO₂CF₂H Br 3-CF₃ Br 3-OCF₃Br 3-OCF₂H Br 3-OCF₂CF₂H Br 3-OCH₂CF₃ Br 3-SCF₃ Br 3-SOCF₃ Br 3-SO₂CF₃Br 3-SCF₂H Br 3-SOCF₂H Br 3-SO₂CF₂H I 3-CF₃ I 3-OCF₃ I 3-OCF₂H I3-OCF₂CF₂H I 3-OCH₂CF₃ I 3-SCF₃ I 3-SOCF₃ I 3-SO₂CF₃ I 3-SCF₂H I3-SOCF₂H I 3-SO₂CF₂H OMe 3-CF₃ OMe 3-OCF₃ OMe 3-OCF₂H OMe 3-OCF₂CF₂H OMe3-OCH₂CF₃ OMe 3-SCF₃ OMe 3-SOCF₃ OMe 3-SO₂CF₃ OMe 3-SCF₂H OMe 3-SOCF₂HOMe 3-SO₂CF₂H CF₃ 3-CF₃ CF₃ 3-OCF₃ CF₃ 3-OCF₂H CF₃ 3-OCF₂CF₂H CF₃3-OCH₂CF₃ CF₃ 3-SCF₃ CF₃ 3-SOCF₃ CF₃ 3-SO₂CF₃ CF₃ 3-SCF₂H CF₃ 3-SOCF₂HCF₃ 3-SO₂CF₂H OCF₂H 3-CF₃ OCF₂H 3-OCF₃ OCF₂H 3-OCF₂H OCF₂H 3-OCF₂CF₂HOCF₂H 3-OCH₂CF₃ OCF₂H 3-SCF₃ OCF₂H 3-SOCF₃ OCF₂H 3-SO₂CF₃ OCF₂H 3-SCF₂HOCF₂H 3-SOCF₂H OCF₂H 3-SO₂CF₂H F 2-Me-4-CF₃ F 2-Me-4-OCF₃ F 2-Me-4-OCF₂HF 2-Me-4-OCH₂CF₃ F 2-Me-4-SCF₃ F 2-Me-4-SOCF₃ F 2-Me-4-SO₂CF₃ F2-Me-4-SCF₂H F 2-Me-4-SOCF₂H F 2-Me-4-SO₂CF₂H I 2-Me-4-CF₃ I 2-Me-4-OCF₃I 2-Me-4-OCF₂H I 2-Me-4-OCH₂CF₃ I 2-Me-4-SCF₃ I 2-Me-4-SOCF₃ I2-Me-4-SO₂CF₃ I 2-Me-4-SCF₂H I 2-Me-4-SOCF₂H I 2-Me-4-SO₂CF₂H NO₂2-Me-4-CF₃ NO₂ 2-Me-4-OCF₃ NO₂ 2-Me-4-OCF₂H NO₂ 2-Me-4-OCH₂CF₃ NO₂2-Me-4-SCF₃ NO₂ 2-Me-4-SOCF₃ NO₂ 2-Me-4-SO₂CF₃ NO₂ 2-Me-4-SCF₂H NO₂2-Me-4-SOCF₂H NO₂ 2-Me-4-SO₂CF₂H Me 4-CF₃ Me 4-OCF₃ Me 4-OCF₂H Me4-OCF₂CF₂H Me 4-OCH₂CF₃ Me 4-SCF₃ Me 4-SOCF₃ Me 4-SO₂CF₃ Me 4-SCF₂H Me4-SOCF₂H Me 4-SO₂CF₂H Cl 4-CF₃ Cl 4-OCF₃ Cl 4-OCF₂H Cl 4-OCF₂CF₂H Cl4-OCH₂CF₃ Cl 4-SCF₃ Cl 4-SOCF₃ Cl 4-SO₂CF₃ Cl 4-SCF₂H Cl 4-SOCF₂H Cl4-SO₂CF₂H F 4-CF₃ F 4-OCF₃ F 4-OCF₂H F 4-OCF₂CF₂H F 4-OCH₂CF₃ F 4-SCF₃ F4-SOCF₃ F 4-SO₂CF₃ F 4-SCF₂H F 4-SOCF₂H F 4-SO₂CF₂H Br 4-CF₃ Br 4-OCF₃Br 4-OCF₂H Br 4-OCF₂CF₂H Br 4-OCH₂CF₃ Br 4-SCF₃ Br 4-SOCF₃ Br 4-SO₂CF₃Br 4-SCF₂H Br 4-SOCF₂H Br 4-SO₂CF₂H I 4-CF₃ I 4-OCF₃ I 4-OCF₂H I4-OCF₂CF₂H I 4-OCH₂CF₃ I 4-SCF₃ I 4-SOCF₃ I 4-SO₂CF₃ I 4-SCF₂H I4-SOCF₂H I 4-SO₂CF₂H OMe 4-CF₃ OMe 4-OCF₃ OMe 4-OCF₂H OMe 4-OCF₂CF₂H OMe4-OCH₂CF₃ OMe 4-SCF₃ OMe 4-SOCF₃ OMe 4-SO₂CF₃ OMe 4-SCF₂H OMe 4-SOCF₂HOMe 4-SO₂CF₂H CF₃ 4-CF₃ CF₃ 4-OCF₃ CF₃ 4-OCF₂H CF₃ 4-OCF₂CF₂H CF₃4-OCH₂CF₃ CF₃ 4-SCF₃ CF₃ 4-SOCF₃ CF₃ 4-SO₂CF₃ CF₃ 4-SCF₂H CF₃ 4-SOCF₂HCF₃ 4-SO₂CF₂H OCF₂H 4-CF₃ OCF₂H 4-OCF₃ OCF₂H 4-OCF₂H OCF₂H 4-OCF₂CF₂HOCF₂H 4-OCH₂CF₃ OCF₂H 4-SCF₃ OCF₂H 4-SOCF₃ OCF₂H 4-SO₂CF₃ OCF₂H 4-SCF₂HOCF₂H 4-SOCF₂H OCF₂H 4-SO₂CF₂H Cl 2-Me-4-CF₃ Cl 2-Me-4-OCF₃ Cl2-Me-4-OCF₂H Cl 2-Me-4-OCH₂CF₃ Cl 2-Me-4-SCF₃ Cl 2-Me-4-SOCF₃ Cl2-Me-4-SO₂CF₃ Cl 2-Me-4-SCF₂H Cl 2-Me-4-SOCF₂H Cl 2-Me-4-SO₂CF₂H OMe2-Me-4-CF₃ OMe 2-Me-4-OCF₃ OMe 2-Me-4-OCF₂H OMe 2-Me-4-OCH₂CF₃ OMe2-Me-4-SCF₃ OMe 2-Me-4-SOCF₃ OMe 2-Me-4-SO₂CF₃ OMe 2-Me-4-SCF₂H OMe2-Me-4-SOCF₂H OMe 2-Me-4-SO₂CF₂H SMe 2-Me-4-CF₃ SMe 2-Me-4-OCF₃ SMe2-Me-4-OCF₂H SMe 2-Me-4-OCH₂CF₃ SMe 2-Me-4-SCF₃ SMe 2-Me-4-SOCF₃ SMe2-Me-4-SO₂CF₃ SMe 2-Me-4-SCF₂H SMe 2-Me-4-SOCF₂H SMe 2-Me-4-SO₂CF₂H

[0340] TABLE 4

R⁴ R⁵ and/or R⁶ Me 2-CF₃ Me 2-OCF₃ Me 2-OCF₂H Me 2-OCF₂CF₂H Me 2-OCH₂CF₃Me 2-SCF₃ Me 2-SOCF₃ Me 2-SO₂CF₃ Me 2-SCF₂H Me 2-SOCF₂H Me 2-SO₂CF₂H Cl2-CF₃ Cl 2-OCF₃ Cl 2-OCF₂H Cl 2-OCF₂CF₂H Cl 2-OCH₂CF₃ Cl 2-SCF₃ Cl2-SOCF₃ Cl 2-SO₂CF₃ Cl 2-SCF₂H Cl 2-SOCF₂H Cl 2-SO₂CF₂H F 2-CF₃ F 2-OCF₃F 2-OCF₂H F 2-OCF₂CF₂H F 2-OCH₂CF₃ F 2-SCF₃ F 2-SOCF₃ F 2-SO₂CF₃ F2-SCF₂H F 2-SOCF₂H F 2-SO₂CF₂H Br 2-CF₃ Br 2-OCF₃ Br 2-OCF₂H Br2-OCF₂CF₂H Br 2-OCH₂CF₃ Br 2-SCF₃ Br 2-SOCF₃ Br 2-SO₂CF₃ Br 2-SCF₂H Br2-SOCF₂H Br 2-SO₂CF₂H I 2-CF₃ I 2-OCF₃ I 2-OCF₂H I 2-OCF₂CF₂H I2-OCH₂CF₃ I 2-SCF₃ I 2-SOCF₃ I 2-SO₂CF₃ I 2-SCF₂H I 2-SOCF₂H I 2-SO₂CF₂HOMe 2-CF₃ OMe 2-OCF₃ OMe 2-OCF₂H OMe 2-OCF₂CF₂H OMe 2-OCH₂CF₃ OMe 2-SCF₃OMe 2-SOCF₃ OMe 2-SO₂CF₃ OMe 2-SCF₂H OMe 2-SOCF₂H OMe 2-SO₂CF₂H CF₃2-CF₃ CF₃ 2-OCF₃ CF₃ 2-OCF₂H CF₃ 2-OCF₂CF₂H CF₃ 2-OCH₂CF₃ CF₃ 2-SCF₃ CF₃2-SOCF₃ CF₃ 2-SO₂CF₃ CF₃ 2-SCF₂H CF₃ 2-SOCF₂H CF₃ 2-SO₂CF₂H OCF₂H 2-CF₃OCF₂H 2-OCF₃ OCF₂H 2-OCF₂H OCF₂H 2-OCF₂CF₂H OCF₂H 2-OCH₂CF₃ OCF₂H 2-SCF₃OCF₂H 2-SOCF₃ OCF₂H 2-SO₂CF₃ OCF₂H 2-SCF₂H OCF₂H 2-SOCF₂H OCF₂H2-SO₂CF₂H Me 2-Me-4-CF₃ Me 2-Me-4-OCF₃ Me 2-Me-4-OCF₂H Me 2-Me-4-OCH₂CF₃Me 2-Me-4-SCF₃ Me 2-Me-4-SOCF₃ Me 2-Me-4-SO₂CF₃ Me 2-Me-4-SCF₂H Me2-Me-4-SOCF₂H Me 2-Me-4-SO₂CF₂H Br 2-Me-4-CF₃ Br 2-Me-4-OCF₃ Br2-Me-4-OCF₂H Br 2-Me-4-OCH₂CF₃ Br 2-Me-4-SCF₃ Br 2-Me-4-SOCF₃ Br2-Me-4-SO₂CF₃ Br 2-Me-4-SCF₂H Br 2-Me-4-SOCF₂H Br 2-Me-4-SO₂CF₂H CF₃2-Me-4-CF₃ CF₃ 2-Me-4-OCF₃ CF₃ 2-Me-4-OCF₂H CF₃ 2-Me-4-OCH₂CF₃ CF₃2-Me-4-SCF₃ CF₃ 2-Me-4-SOCF₃ CF₃ 2-Me-4-SO₂CF₃ CF₃ 2-Me-4-SCF₂H CF₃2-Me-4-SOCF₂H CF₃ 2-Me-4-SO₂CF₂H Me 3-CF₃ Me 3-OCF₃ Me 3-OCF₂H Me3-OCF₂CF₂H Me 3-OCH₂CF₃ Me 3-SCF₃ Me 3-SOCF₃ Me 3-SO₂CF₃ Me 3-SCF₂H Me3-SOCF₂H Me 3-SO₂CF₂H Cl 3-CF₃ Cl 3-OCF₃ Cl 3-OCF₂H Cl 3-OCF₂CF₂H Cl3-OCH₂CF₃ Cl 3-SCF₃ Cl 3-SOCF₃ Cl 3-SO₂CF₃ Cl 3-SCF₂H Cl 3-SOCF₂H Cl3-SO₂CF₂H F 3-CF₃ F 3-OCF₃ F 3-OCF₂H F 3-OCF₂CF₂H F 3-OCH₂CF₃ F 3-SCF₃ F3-SOCF₃ F 3-SO₂CF₃ F 3-SCF₂H F 3-SOCF₂H F 3-SO₂CF₂H Br 3-CF₃ Br 3-OCF₃Br 3-OCF₂H Br 3-OCF₂CF₂H Br 3-OCH₂CF₃ Br 3-SCF₃ Br 3-SOCF₃ Br 3-SO₂CF₃Br 3-SCF₂H Br 3-SOCF₂H Br 3-SO₂CF₂H I 3-CF₃ I 3-OCF₃ I 3-OCF₂H I3-OCF₂CF₂H I 3-OCH₂CF₃ I 3-SCF₃ I 3-SOCF₃ I 3-SO₂CF₃ I 3-SCF₂H I3-SOCF₂H I 3-SO₂CF₂H OMe 3-CF₃ OMe 3-OCF₃ OMe 3-OCF₂H OMe 3-OCF₂CF₂H OMe3-OCH₂CF₃ OMe 3-SCF₃ OMe 3-SOCF₃ OMe 3-SO₂CF₃ OMe 3-SCF₂H OMe 3-SOCF₂HOMe 3-SO₂CF₂H CF₃ 3-CF₃ CF₃ 3-OCF₃ CF₃ 3-OCF₂H CF₃ 3-OCF₂CF₂H CF₃3-OCH₂CF₃ CF₃ 3-SCF₃ CF₃ 3-SOCF₃ CF₃ 3-SO₂CF₃ CF₃ 3-SCF₂H CF₃ 3-SOCF₂HCF₃ 3-SO₂CF₂H OCF₂H 3-CF₃ OCF₂H 3-OCF₃ OCF₂H 3-OCF₂H OCF₂H 3-OCF₂CF₂HOCF₂H 3-OCH₂CF₃ OCF₂H 3-SCF₃ OCF₂H 3-SOCF₃ OCF₂H 3-SO₂CF₃ OCF₂H 3-SCF₂HOCF₂H 3-SOCF₂H OCF₂H 3-SO₂CF₂H F 2-Me-4-CF₃ F 2-Me-4-OCF₃ F 2-Me-4-OCF₂HF 2-Me-4-OCH₂CF₃ F 2-Me-4-SCF₃ F 2-Me-4-SOCF₃ F 2-Me-4-SO₂CF₃ F2-Me-4-SCF₂H F 2-Me-4-SOCF₂H F 2-Me-4-SO₂CF₂H I 2-Me-4-CF₃ I 2-Me-4-OCF₃I 2-Me-4-OCF₂H I 2-Me-4-OCH₂CF₃ I 2-Me-4-SCF₃ I 2-Me-4-SOCF₃ I2-Me-4-SO₂CF₃ I 2-Me-4-SCF₂H I 2-Me-4-SOCF₂H I 2-Me-4-SO₂CF₂H NO₂2-Me-4-CF₃ NO₂ 2-Me-4-OCF₃ NO₂ 2-Me-4-OCF₂H NO₂ 2-Me-4-OCH₂CF₃ NO₂2-Me-4-SCF₃ NO₂ 2-Me-4-SOCF₃ NO₂ 2-Me-4-SO₂CF₃ NO₂ 2-Me-4-SCF₂H NO₂2-Me-4-SOCF₂H NO₂ 2-Me-4-SO₂CF₂H Me 4-CF₃ Me 4-OCF₃ Me 4-OCF₂H Me4-OCF₂CF₂H Me 4-OCH₂CF₃ Me 4-SCF₃ Me 4-SOCF₃ Me 4-SO₂CF₃ Me 4-SCF₂H Me4-SOCF₂H Me 4-SO₂CF₂H Cl 4-CF₃ Cl 4-OCF₃ Cl 4-OCF₂H Cl 4-OCF₂CF₂H Cl4-OCH₂CF₃ Cl 4-SCF₃ Cl 4-SOCF₃ Cl 4-SO₂CF₃ Cl 4-SCF₂H Cl 4-SOCF₂H Cl4-SO₂CF₂H F 4-CF₃ F 4-OCF₃ F 4-OCF₂H F 4-OCF₂CF₂H F 4-OCH₂CF₃ F 4-SCF₃ F4-SOCF₃ F 4-SO₂CF₃ F 4-SCF₂H F 4-SOCF₂H F 4-SO₂CF₂H Br 4-CF₃ Br 4-OCF₃Br 4-OCF₂H Br 4-OCF₂CF₂H Br 4-OCH₂CF₃ Br 4-SCF₃ Br 4-SOCF₃ Br 4-SO₂CF₃Br 4-SCF₂H Br 4-SOCF₂H Br 4-SO₂CF₂H I 4-CF₃ I 4-OCF₃ I 4-OCF₂H I4-OCF₂CF₂H I 4-OCH₂CF₃ I 4-SCF₃ I 4-SOCF₃ I 4-SO₂CF₃ I 4-SCF₂H I4-SOCF₂H I 4-SO₂CF₂H OMe 4-CF₃ OMe 4-OCF₃ OMe 4-OCF₂H OMe 4-OCF₂CF₂H OMe4-OCH₂CF₃ OMe 4-SCF₃ OMe 4-SOCF₃ OMe 4-SO₂CF₃ OMe 4-SCF₂H OMe 4-SOCF₂HOMe 4-SO₂CF₂H CF₃ 4-CF₃ CF₃ 4-OCF₃ CF₃ 4-OCF₂H CF₃ 4-OCF₂CF₂H CF₃4-OCH₂CF₃ CF₃ 4-SCF₃ CF₃ 4-SOCF₃ CF₃ 4-SO₂CF₃ CF₃ 4-SCF₂H CF₃ 4-SOCF₂HCF₃ 4-SO₂CF₂H OCF₂H 4-CF₃ OCF₂H 4-OCF₃ OCF₂H 4-OCF₂H OCF₂H 4-OCF₂CF₂HOCF₂H 4-OCH₂CF₃ OCF₂H 4-SCF₃ OCF₂H 4-SOCF₃ OCF₂H 4-SO₂CF₃ OCF₂H 4-SCF₂HOCF₂H 4-SOCF₂H OCF₂H 4-SO₂CF₂H Cl 2-Me-4-CF₃ Cl 2-Me-4-OCF₃ Cl2-Me-4-OCF₂H Cl 2-Me-4-OCH₂CF₃ Cl 2-Me-4-SCF₃ Cl 2-Me-4-SOCF₃ Cl2-Me-4-SO₂CF₃ Cl 2-Me-4-SCF₂H Cl 2-Me-4-SOCF₂H Cl 2-Me-4-SO₂CF₂H OMe2-Me-4-CF₃ OMe 2-Me-4-OCF₃ OMe 2-Me-4-OCF₂H OMe 2-Me-4-OCH₂CF₃ OMe2-Me-4-SCF₃ OMe 2-Me-4-SOCF₃ OMe 2-Me-4-SO₂CF₃ OMe 2-Me-4-SCF₂H OMe2-Me-4-SOCF₂H OMe 2-Me-4-SO₂CF₂H SMe 2-Me-4-CF₃ SMe 2-Me-4-OCF₃ SMe2-Me-4-OCF₂H SMe 2-Me-4-OCH₂CF₃ SMe 2-Me-4-SCF₃ SMe 2-Me-4-SOCF₃ SMe2-Me-4-SO₂CF₃ SMe 2-Me-4-SCF₂H SMe 2-Me-4-SOCF₂H SMe 2-Me-4-SO₂CF₂H

[0341] TABLE 5

R³ R⁴ R⁷ W X Y Z i-Pr Me CF₃ CMe N CH CH i-Pr Cl CF₃ CMe N CH CH i-Pr BrCF₃ CMe N CH CH i-Pr I CF₃ CMe N CH CH i-Pr F CF₃ CMe N CH CH i-Pr H CF₃CMe N CH CH i-Pr Et CF₃ CMe N CH CH i-Pr Me CF₃ CMe CH N CH i-Pr Cl CF₃CMe CH N CH i-Pr Br CF₃ CMe CH N CH i-Pr I CF₃ CMe CH N CH i-Pr F CF₃CMe CH N CH i-Pr H CF₃ CMe CH N CH i-Pr Et CF₃ CMe CH N CH i-Pr Me CF₃CMe CH CH N i-Pr Cl CF₃ CMe CH CH N i-Pr Br CF₃ CMe CH CH N i-Pr I CF₃CMe CH CH N i-Pr F CF₃ CMe CH CH N i-Pr H CF₃ CMe CH CH N i-Pr Et CF₃CMe CH CH N i-Pr Me CF₃ CMe N CH N i-Pr Cl CF₃ CMe N CH N i-Pr Br CF₃CMe N CH N i-Pr I CF₃ CMe N CH N i-Pr F CF₃ CMe N CH N i-Pr H CF₃ CMe NCH N i-Pr Et CF₃ CMe N CH N t-Bu Me CF₃ CMe N CH CH t-Bu Cl CF₃ CMe N CHCH t-Bu Br CF₃ CMe N CH CH t-Bu I CF₃ CMe N CH CH t-Bu F CF₃ CMe N CH CHt-Bu H CF₃ CMe N CH CH t-Bu Et CF₃ CMe N CH CH t-Bu Me CF₃ CMe CH N CHt-Bu Cl CF₃ CMe CH N CH t-Bu Br CF₃ CMe CH N CH t-Bu I CF₃ CMe CH N CHt-Bu F CF₃ CMe CH N CH t-Bu H CF₃ CMe CH N CH t-Bu Et CF₃ CMe CH N CHt-Bu Me CF₃ CMe CH CH N t-Bu Cl CF₃ CMe CH CH N t-Bu Br CF₃ CMe CH CH Nt-Bu I CF₃ CMe CH CH N t-Bu F CF₃ CMe CH CH N t-Bu H CF₃ CMe CH CH Nt-Bu Et CF₃ CMe CH CH N i-Pr Me OCF₃ CMe N CH CH i-Pr Cl OCF₃ CMe N CHCH i-Pr Br OCF₃ CMe N CH CH i-Pr I OCF₃ CMe N CH CH i-Pr F OCF₃ CMe N CHCH i-Pr H OCF₃ CMe N CH CH i-Pr Et OCF₃ CMe N CH CH i-Pr Me CF₃ CH N CHCH i-Pr Cl CF₃ CH N CH CH i-Pr Br CF₃ CH N CH CH i-Pr I CF₃ CH N CH CHi-Pr F CF₃ CH N CH CH i-Pr H CF₃ CH N CH CH i-Pr Et CF₃ CH N CH CH i-PrMe Cl CMe CH CH N i-Pr Cl Cl CMe CH CH N i-Pr Br Cl CMe CH CH N i-Pr ICl CMe CH CH N i-Pr F Cl CMe CH CH N i-Pr H Cl CMe CH CH N i-Pr Et ClCMe CH CH N

[0342] TABLE 6

R³ R⁴ R⁷ X Y Z i-Pr Me CF₃ CMe N CH i-Pr Cl CF₃ CMe N CH i-Pr Br CF₃ CMeN CH i-Pr I CF₃ CMe N CH i-Pr F CF₃ CMe N CH i-Pr H CF₃ CMe N CH i-Pr EtCF₃ CMe N CH i-Pr Me CF₃ CMe CH N i-Pr Cl CF₃ CMe CH N i-Pr Br CF₃ CMeCH N i-Pr I CF₃ CMe CH N i-Pr F CF₃ CMe CH N i-Pr H CF₃ CMe CH N i-Pr EtCF₃ CMe CH N i-Pr Me CF₃ CMe N N i-Pr Cl CF₃ CMe N N i-Pr Br CF₃ CMe N Ni-Pr I CF₃ CMe N N i-Pr F CF₃ CMe N N i-Pr H CF₃ CMe N N i-Pr Et CF₃ CMeN N i-Pr Me CF₃ CEt CH N i-Pr Cl CF₃ CEt CH N i-Pr Br CF₃ CEt CH N i-PrI CF₃ CEt CH N i-Pr F CF₃ CEt CH N i-Pr H CF₃ CEt CH N i-Pr Et CF₃ CEtCH N t-Bu Me CF₃ CMe N CH t-Bu Cl CF₃ CMe N CH t-Bu Br CF₃ CMe N CH t-BuI CF₃ CMe N CH t-Bu F CF₃ CMe N CH t-Bu H CF₃ CMe N CH t-Bu Et CF₃ CMe NCH t-Bu Me CF₃ CMe CH N t-Bu Cl CF₃ CMe CH N t-Bu Br CF₃ CMe CH N t-Bu ICF₃ CMe CH N t-Bu F CF₃ CMe CH N t-Bu H CF₃ CMe CH N t-Bu Et CF₃ CMe CHN t-Bu Me CF₃ CMe N N t-Bu Cl CF₃ CMe N N t-Bu Br CF₃ CMe N N t-Bu I CF₃CMe N N t-Bu F CF₃ CMe N N t-Bu H CF₃ CMe N N t-Bu Et CF₃ CMe N N i-PrMe OCF₃ CMe CH N i-Pr Cl OCF₃ CMe CH N i-Pr Br OCF₃ CMe CH N i-Pr I OCF₃CMe CH N i-Pr F OCF₃ CMe CH N i-Pr H OCF₃ CMe CH N i-Pr Et OCF₃ CMe CH Ni-Pr Me CF₃ CH CH N i-Pr Cl CF₃ CH CH N i-Pr Br CF₃ CH CH N i-Pr I CF₃CH CH N i-Pr F CF₃ CH CH N i-Pr H CF₃ CH CH N i-Pr Et CF₃ CH CH N i-PrMe Cl CMe CH N i-Pr Cl Cl CMe CH N i-Pr Br Cl CMe CH N i-Pr I Cl CMe CHN i-Pr F Cl CMe CH N i-Pr H Cl CMe CH N i-Pr Et Cl CMe CH N

[0343] TABLE 7

R³ R⁴ Q X Y Z i-Pr Me S CCF₃ CH CH i-Pr Cl S CCF₃ CH CH i-Pr Br S CCF₃CH CH i-Pr I S CCF₃ CH CH i-Pr F S CCF₃ CH CH i-Pr H S CCF₃ CH CH i-PrEt S CCF₃ CH CH i-Pr Me S CCF₃ CMe CH i-Pr Cl S CCF₃ CMe CH i-Pr Br SCCF₃ CMe CH i-Pr I S CCF₃ CMe CH i-Pr F S CCF₃ CMe CH i-Pr H S CCF₃ CMeCH i-Pr Et S CCF₃ CMe CH t-Bu Me S CCF₃ CMe CH t-Bu Cl S CCF₃ CMe CHt-Bu Br S CCF₃ CMe CH t-Bu I S CCF₃ CMe CH t-Bu F S CCF₃ CMe CH t-Bu H SCCF₃ CMe CH t-Bu Et S CCF₃ CMe CH i-Pr Me S CCF₃ CMe N i-Pr Cl S CCF₃CMe N i-Pr Br S CCF₃ CMe N i-Pr I S CCF₃ CMe N i-Pr F S CCF₃ CMe N i-PrH S CCF₃ CMe N i-Pr Et S CCF₃ CMe N i-Pr Me S COCH₂CF₃ CMe N i-Pr Cl SCOCH₂CF₃ CMe N i-Pr Br S COCH₂CF₃ CMe N i-Pr I S COCH₂CF₃ CMe N i-Pr F SCOCH₂CF₃ CMe N i-Pr H S COCH₂CF₃ CMe N i-Pr Et S COCH₂CF₃ CMe N i-Pr MeS COCHF₂ CMe N i-Pr Cl S COCHF₂ CMe N i-Pr Br S COCHF₂ CMe N i-Pr I SCOCHF₂ CMe N i-Pr F S COCHF₂ CMe N i-Pr H S COCHF₂ CMe N i-Pr Et SCOCHF₂ CMe N i-Pr Me O CCF₃ CMe N i-Pr Cl O CCF₃ CMe N i-Pr Br O CCF₃CMe N i-Pr I O CCF₃ CMe N i-Pr F O CCF₃ CMe N i-Pr H O CCF₃ CMe N i-PrEt O CCF₃ CMe N i-Pr Me NMe N CH CCF₃ i-Pr Cl NMe N CH CCF₃ i-Pr Br NMeN CH CCF₃ i-Pr I NMe N CH CCF₃ i-Pr F NMe N CH CCF₃ i-Pr H NMe N CH CCF₃i-Pr Et NMe N CH CCF₃ i-Pr Me NEt N CH CCF₃ i-Pr Cl NEt N CH CCF₃ i-PrBr NEt N CH CCF₃ i-Pr I NEt N CH CCF₃ i-Pr F NEt N CH CCF₃ i-Pr H NEt NCH CCF₃ i-Pr Et NEt N CH CCF₃ i-Pr Me NMe N CH CC₂F₃ i-Pr Cl NMe N CHCC₂F₃ i-Pr Br NMe N CH CCF₃ i-Pr I NMe N CH CCF₃ i-Pr F NMe N CH CCF₃i-Pr H NMe N CH CCF₃ i-Pr Et NMe N CH CCF₃ t-Bu Me NMe N CH CCF₃ t-Bu ClNMe N CH CCF₃ t-Bu Br NMe N CH CCF₃ t-Bu I NMe N CH CCF₃ t-Bu F NMe N CHCCF₃ t-Bu H NMe N CH CCF₃ t-Bu Et NMe N CH CCF₃ i-Pr Me NMe CH N CCF₃i-Pr Cl NMe CH N CCF₃ i-Pr Br NMe CH N CCF₃ i-Pr I NMe CH N CCF₃ i-Pr FNMe CH N CCF₃ i-Pr H NMe CH N CCF₃ i-Pr Et NMe CH N CCF₃ i-Pr Me NMe N NCCF₃ i-Pr Cl NMe N N CCF₃ i-Pr Br NMe N N CCF₃ i-Pr I NMe N N CCF₃ i-PrF NMe N N CCF₃ i-Pr H NMe N N CCF₃ i-Pr Et NMe N N CCF₃

[0344] TABLE 8

R³ R⁴ Q X Y Z i-Pr Me NCHF₂ CMe N CH i-Pr Cl NCHF₂ CMe N CH i-Pr BrNCHF₂ CMe N CH i-Pr I NCHF₂ CMe N CH i-Pr F NCHF₂ CMe N CH i-Pr H NCHF₂CMe N CH i-Pr Et NCHF₂ CMe N CH i-Pr Me NCHF₂ CH N CMe i-Pr Cl NCHF₂ CHN CMe i-Pr Br NCHF₂ CH N CMe i-Pr I NCHF₂ CH N CMe i-Pr F NCHF₂ CH N CMei-Pr H NCHF₂ CH N CMe i-Pr Et NCHF₂ CH N CMe i-Pr Me NCF₂CHF₂ CMe N CHi-Pr Cl NCF₂CHF₂ CMe N CH i-Pr Br NCF₂CHF₂ CMe N CH i-Pr I NCF₂CHF₂ CMeN CH i-Pr F NCF₂CHF₂ CMe N CH i-Pr H NCF₂CHF₂ CMe N CH i-Pr Et NCF₂CHF₂CMe N CH i-Pr Me NCF₂CHF₂ CH N CMe i-Pr Cl NCF₂CHF₂ CH N CMe i-Pr BrNCF₂CHF₂ CH N CMe i-Pr I NCF₂CHF₂ CH N CMe i-Pr F NCF₂CHF₂ CH N CMe i-PrH NCF₂CHF₂ CH N CMe i-Pr Et NCF₂CHF₂ CH N CMe i-Pr Me NCH₂CF₃ CMe N CHi-Pr Cl NCH₂CF₃ CMe N CH i-Pr Br NCH₂CF₃ CMe N CH i-Pr I NCH₂CF₃ CMe NCH i-Pr F NCH₂CF₃ CMe N CH i-Pr H NCH₂CF₃ CMe N CH i-Pr Et NCH₂CF₃ CMe NCH i-Pr Me NCH₂CF₃ CH N CMe i-Pr Cl NCH₂CF₃ CH N CMe i-Pr Br NCH₂CF₃ CHN CMe i-Pr I NCH₂CF₃ CH N CMe i-Pr F NCH₂CF₃ CH N CMe i-Pr H NCH₂CF₃ CHN CMe i-Pr Et NCH₂CF₃ CH N CMe i-Pr Me NCF₂CHF₂ N CH CMe i-Pr ClNCF₂CHF₂ N CH CMe i-Pr Br NCF₂CHF₂ N CH CMe i-Pr I NCF₂CHF₂ N CH CMei-Pr F NCF₂CHF₂ N CH CMe i-Pr H NCF₂CHF₂ N CH CMe i-Pr Et NCF₂CHF₂ N CHCMe

[0345] TABLE 9

W X Y Z R³ R⁴ R⁷ R⁸ CH CH CH CH i-Pr Me CF₃ Me CH CH CH CH t-Bu Me CF₃Me CH CH CH CH i-Pr Cl CF₃ Me CH CH CH CH t-Bu Cl CF₃ Me CH CH CH CHi-Pr Br CF₃ Me CH CH CH CH t-Bu Br CF₃ Me CH CH CH CH i-Pr Me Cl Me CHCH CH CH t-Bu Me Cl Me CH CH CH CH i-Pr Cl Cl Me CH CH CH CH t-Bu Cl ClMe CH CH CH CH i-Pr Br Cl Me CH CH CH CH t-Bu Br Cl Me CH CH CH CH i-PrMe Br Me CH CH CH CH t-Bu Me Br Me CH CH CH CH i-Pr Cl Br Me CH CH CH CHt-Bu Cl Br Me CH CH CH CH i-Pr Br Br Me CH CH CH CH t-Bu Br Br Me CH CHCH CH i-Pr Me CN Me CH CH CH CH t-Bu Me CN Me CH CH CH CH i-Pr Cl CN MeCH CH CH CH t-Bu Cl CN Me CH CH CH CH i-Pr Br CN Me CH CH CH CH t-Bu BrCN Me CH CH CH CH i-Pr Me CF₃ F CH CH CH CH t-Bu Me CF₃ F CH CH CH CHi-Pr Cl CF₃ F CH CH CH CH t-Bu Cl CF₃ F CH CH CH CH i-Pr Br CF₃ F CH CHCH CH t-Bu Br CF₃ F CH CH CH CH i-Pr Me Cl F CH CH CH CH t-Bu Me Cl F CHCH CH CH i-Pr Cl Cl F CH CH CH CH t-Bu Cl Cl F CH CH CH CH i-Pr Br Cl FCH CH CH CH t-Bu Br Cl F CH CH CH CH i-Pr Me Br F CH CH CH CH t-Bu Me BrF CH CH CH CH i-Pr Cl Br F CH CH CH CH t-Bu Cl Br F CH CH CH CH i-Pr BrBr F CH CH CH CH t-Bu Br Br F CH CH CH CH i-Pr Me CN F CH CH CH CH t-BuMe CN F CH CH CH CH i-Pr Cl CN F CH CH CH CH t-Bu Cl CN F CH CH CH CHi-Pr Br CN F CH CH CH CH t-Bu Br CN F CH CH CH CH i-Pr Me CF₃ Cl CH CHCH CH t-Bu Me CF₃ Cl CH CH CH CH i-Pr Cl CF₃ Cl CH CH CH CH t-Bu Cl CF₃Cl CH CH CH CH i-Pr Br CF₃ Cl CH CH CH CH t-Bu Br CF₃ Cl CH CH CH CHi-Pr Me Cl Cl CH CH CH CH t-Bu Me Cl Cl CH CH CH CH i-Pr Cl Cl Cl CH CHCH CH t-Bu Cl Cl Cl CH CH CH CH i-Pr Br Cl Cl CH CH CH CH t-Bu Br Cl ClCH CH CH CH i-Pr Me Br Cl CH CH CH CH t-Bu Me Br Cl CH CH CH CH i-Pr ClBr Cl CH CH CH CH t-Bu Cl Br Cl CH CH CH CH i-Pr Br Br Cl CH CH CH CHt-Bu Br Br Cl CH CH CH CH i-Pr Me CN Cl CH CH CH CH t-Bu Me CN Cl CH CHCH CH i-Pr Cl CN Cl CH CH CH CH t-Bu Cl CN Cl CH CH CH CH i-Pr Br CN ClCH CH CH CH t-Bu Br CN Cl CH CH CH CH i-Pr Me CF₃ Br CH CH CH CH t-Bu MeCF₃ Br CH CH CH CH i-Pr Cl CF₃ Br CH CH CH CH t-Bu Cl CF₃ Br CH CH CH CHi-Pr Br CF₃ Br CH CH CH CH t-Bu Br CF₃ Br CH CH CH CH i-Pr Me Cl Br CHCH CH CH t-Bu Me Cl Br CH CH CH CH i-Pr Cl Cl Br CH CH CH CH t-Bu Cl ClBr CH CH CH CH i-Pr Br Cl Br CH CH CH CH t-Bu Br Cl Br CH CH CH CH i-PrMe Br Br CH CH CH CH t-Bu Me Br Br CH CH CH CH i-Pr Cl Br Br CH CH CH CHt-Bu Cl Br Br CH CH CH CH i-Pr Br Br Br CH CH CH CH t-Bu Br Br Br CH CHCH CH i-Pr Me CN Br CH CH CH CH t-Bu Me CN Br CH CH CH CH i-Pr Cl CN BrCH CH CH CH t-Bu Cl CN Br CH CH CH CH i-Pr Br CN Br CH CH CH CH t-Bu BrCN Br CH CH CH CH i-Pr Me CF₃ CN CH CH CH CH t-Bu Me CF₃ CN CH CH CH CHi-Pr Cl CF₃ CN CH CH CH CH t-Bu Cl CF₃ CN CH CH CH CH i-Pr Br CF₃ CN CHCH CH CH t-Bu Br CF₃ CN CH CH CH CH i-Pr Me Cl CN CH CH CH CH t-Bu Me ClCN CH CH CH CH i-Pr Cl Cl CN CH CH CH CH t-Bu Cl Cl CN CH CH CH CH i-PrBr Cl CN CH CH CH CH t-Bu Br Cl CN CH CH CH CH i-Pr Me Br CN CH CH CH CHt-Bu Me Br CN CH CH CH CH i-Pr Cl Br CN CH CH CH CH t-Bu Cl Br CN CH CHCH CH i-Pr Br Br CN CH CH CH CH t-Bu Br Br CN CH CH CH CH i-Pr Me CN CNCH CH CH CH t-Bu Me CN CN CH CH CH CH i-Pr Cl CN CN CH CH CH CH t-Bu ClCN CN CH CH CH CH i-Pr Br CN CN CH CH CH CH t-Bu Br CN CN CH CH CH Ni-Pr Me CF₃ Me CH CH CH N t-Bu Me CF₃ Me CH CH CH N i-Pr Cl CF₃ Me CH CHCH N t-Bu Cl CF₃ Me CH CH CH N i-Pr Br CF₃ Me CH CH CH N t-Bu Br CF₃ MeCH CH CH N i-Pr Me Cl Me CH CH CH N t-Bu Me Cl Me CH CH CH N i-Pr Cl ClMe CH CH CH N t-Bu Cl Cl Me CH CH CH N i-Pr Br Cl Me CH CH CH N t-Bu BrCl Me CH CH CH N i-Pr Me Br Me CH CH CH N t-Bu Me Br Me CH CH CH N i-PrCl Br Me CH CH CH N t-Bu Cl Br Me CH CH CH N i-Pr Br Br Me CH CH CH Nt-Bu Br Br Me CH CH CH N i-Pr Me CN Me CH CH CH N i-Bu Me CN Me CH CH CHN i-Pr Cl CN Me CH CH CH N t-Bu Cl CN Me CH CH CH N i-Pr Br CN Me CH CHCH N t-Bu Br CN Me CH CH CH N i-Pr Me CF₃ F CH CH CH N t-Bu Me CF₃ F CHCH CH N i-Pr Cl CF₃ F CH CH CH N t-Bu Cl CF₃ F CH CH CH N i-Pr Br CF₃ FCH CH CH N t-Bu Br CF₃ F CH CH CH N i-Pr Me Cl F CH CH CH N t-Bu Me Cl FCH CH CH N i-Pr Cl Cl F CH CH CH N t-Bu Cl Cl F CH CH CH N i-Pr Br Cl FCH CH CH N t-Bu Br Cl F CH CH CH N i-Pr Me Br F CH CH CH N t-Bu Me Br FCH CH CH N i-Pr Cl Br F CH CH CH N t-Bu Cl Br F CH CH CH N i-Pr Br Br FCH CH CH N t-Bu Br Br F CH CH CH N i-Pr Me CN F CH CH CH N t-Bu Me CN FCH CH CH N i-Pr Cl CN F CH CH CH N t-Bu Cl CN F CH CH CH N i-Pr Br CN FCH CH CH N t-Bu Br CN F CH CH CH N i-Pr Me CF₃ Cl CH CH CH N t-Bu Me CF₃Cl CH CH CH N i-Pr Cl CF₃ Cl CH CH CH N t-Bu Cl CF₃ Cl CH CH CH N i-PrBr CF₃ Cl CH CH CH N t-Bu Br CF₃ Cl CH CH CH N i-Pr Me Cl Cl CH CH CH Nt-Bu Me Cl Cl CH CH CH N i-Pr Cl Cl Cl CH CH CH N t-Bu Cl Cl Cl CH CH CHN i-Pr Br Cl Cl CH CH CH N t-Bu Br Cl Cl CH CH CH N i-Pr Me Br Cl CH CHCH N t-Bu Me Br Cl CH CH CH N i-Pr Cl Br Cl CH CH CH N t-Bu Cl Br Cl CHCH CH N i-Pr Br Br Cl CH CH CH N t-Bu Br Br Cl CH CH CH N i-Pr Me CN ClCH CH CH N t-Bu Me CN Cl CH CH CH N i-Pr Cl CN Cl CH CH CH N t-Bu Cl CNCl CH CH CH N i-Pr Br CN Cl CH CH CH N t-Bu Br CN Cl CH CH CH N i-Pr MeCF₃ Br CH CH CH N t-Bu Me CF₃ Br CH CH CH N i-Pr Cl CF₃ Br CH CH CH Nt-Bu Cl CF₃ Br CH CH CH N i-Pr Br CF₃ Br CH CH CH N t-Bu Br CF₃ Br CH CHCH N i-Pr Me Cl Br CH CH CH N t-Bu Me Cl Br CH CH CH N i-Pr Cl Cl Br CHCH CH N t-Bu Cl Cl Br CH CH CH N i-Pr Br Cl Br CH CH CH N t-Bu Br Cl BrCH CH CH N i-Pr Me Br Br CH CH CH N t-Bu Me Br Br CH CH CH N i-Pr Cl BrBr CH CH CH N t-Bu Cl Br Br CH CH CH N i-Pr Br Br Br CH CH CH N t-Bu BrBr Br CH CH CH N i-Pr Me CN Br CH CH CH N t-Bu Me CN Br CH CH CH N i-PrCl CN Br CH CH CH N t-Bu Cl CN Br CH CH CH N i-Pr Br CN Br CH CH CH Nt-Bu Br CN Br CH CH CH N i-Pr Me CF₃ CN CH CH CH N t-Bu Me CF₃ CN CH CHCH N i-Pr Cl CF₃ CN CH CH CH N t-Bu Cl CF₃ CN CH CH CH N i-Pr Br CF₃ CNCH CH CH N t-Bu Br CF₃ CN CH CH CH N i-Pr Me Cl CN CH CH CH N t-Bu Me ClCN CH CH CH N i-Pr Cl Cl CN CH CH CH N t-Bu Cl Cl CN CH CH CH N i-Pr BrCl CN CH CH CH N t-Bu Br Cl CN CH CH CH N i-Pr Me Br CN CH CH CH N t-BuMe Br CN CH CH CH N i-Pr Cl Br CN CH CH CH N t-Bu Cl Br CN CH CH CH Ni-Pr Br Br CN CH CH CH N t-Bu Br Br CN CH CH CH N i-Pr Me CN CN CH CH CHN t-Bu Me CN CN CH CH CH N i-Pr Cl CN CN CH CH CH N t-Bu Cl CN CN CH CHCH N i-Pr Br CN CN CH CH CH N t-Bu Br CN CN CH CH CH CH Me Me CF₃ F CHCH CH CH Et Me CF₃ F CH CH CH CH CH(CH₃)CH₂OCH₃ Me CF₃ F CH CH CH CHCH(CH₃)CH₂SCH₃ Me CF₃ F CH CH CH CH propargyl Me CF₃ F CH CH CH CH Me MeCF₃ Cl CH CH CH CH Et Me CF₃ Cl CH CH CH CH CH(CH₃)CH₂OCH₃ Me CF₃ Cl CHCH CH CH CH(CH₃)CH₂SCH₃ Me CF₃ Cl CH CH CH CH propargyl Me CF₃ Cl CH CHCH CH Me Me Br F CH CH CH CH Et Me Br F CH CH CH CH CH(CH₃)CH₂OCH₃ Me BrF CH CH CH CH CH(CH₃)CH₂SCH₃ Me Br F CH CH CH CH propargyl Me Br F CH CHCH CH Me Me Br Cl CH CH CH CH Et Me Br Cl CH CH CH CH CH(CH₃)CH₂OCH₃ MeBr Cl CH CH CH CH CH(CH₃)CH₂SCH₃ Me Br Cl CH CH CH CH propargyl Me Br ClCH CH CH CH Me Cl CF₃ F CH CH CH CH Et Cl CF₃ F CH CH CH CHCH(CH₃)CH₂OCH₃ Cl CF₃ F CH CH CH CH CH(CH₃)CH₂SCH₃ Cl CF₃ F CH CH CH CHpropargyl Cl CF₃ F CH CH CH CH Me Cl CF₃ Cl CH CH CH CH Et Cl CF₃ Cl CHCH CH CH CH(CH₃)CH₂OCH₃ Cl CF₃ Cl CH CH CH CH CH(CH₃)CH₂SCH₃ Cl CF₃ ClCH CH CH CH propargyl Cl CF₃ Cl CH CH CH CH Me Cl Br F CH CH CH CH Et ClBr F CH CH CH CH CH(CH₃)CH₂OCH₃ Cl Br F CH CH CH CH CH(CH₃)CH₂SCH₃ Cl BrF CH CH CH CH propargyl Cl Br F CH CH CH CH Me Cl Br Cl CH CH CH CH EtCl Br Cl CH CH CH CH CH(CH₃)CH₂OCH₃ Cl Br Cl CH CH CH CH CH(CH₃)CH₂SCH₃Cl Br Cl CH CH CH CH propargyl Cl Br Cl CH CH CH N Me Me CF₃ F CH CH CHN Et Me CF₃ F CH CH CH N CH(CH₃)CH₂OCH₃ Me CF₃ F CH CH CH NCH(CH₃)CH₂SCH₃ Me CF₃ F CH CH CH N propargyl Me CF₃ F CH CH CH N Me MeCF₃ Cl CH CH CH N Et Me CF₃ Cl CH CH CH N CH(CH₃)CH₂OCH₃ Me CF₃ Cl CH CHCH N CH(CH₃)CH₂SCH₃ Me CF₃ Cl CH CH CH N propargyl Me CF₃ Cl CH CH CH NMe Me Br F CH CH CH N Et Me Br F CH CH CH N CH(CH₃)CH₂OCH₃ Me Br F CH CHCH N CH(CH₃)CH₂SCH₃ Me Br F CH CH CH N propargyl Me Br F CH CH CH N MeMe Br Cl CH CH CH N Et Me Br Cl CH CH CH N CH(CH₃)CH₂OCH₃ Me Br Cl CH CHCH N CH(CH₃)CH₂SCH₃ Me Br Cl CH CH CH N propargyl Me Br Cl CH CH CH N MeCl CF₃ F CH CH CH N Et Cl CF₃ F CH CH CH N CH(CH₃)CH₂OCH₃ Cl CF₃ F CH CHCH N CH(CH₃)CH₂SCH₃ Cl CF₃ F CH CH CH N propargyl Cl CF₃ F CH CH CH N MeCl CF₃ Cl CH CH CH N Et Cl CF₃ Cl CH CH CH N CH(CH₃)CH₂OCH₃ Cl CF₃ Cl CHCH CH N CH(CH₃)CH₂SCH₃ Cl CF₃ Cl CH CH CH N propargyl Cl CF₃ Cl CH CH CHN Me Cl Br F CH CH CH N Et Cl Br F CH CH CH N CH(CH₃)CH₂OCH₃ Cl Br F CHCH CH N CH(CH₃)CH₂SCH₃ Cl Br F CH CH CH N propargyl Cl Br F CH CH CH NMe Cl Br Cl CH CH CH N Et Cl Br Cl CH CH CH N CH(CH₃)CH₂OCH₃ Cl Br Cl CHCH CH N CH(CH₃)CH₂SCH₃ Cl Br Cl CH CH CH N propargyl Cl Br Cl C—Cl CH CHCH i-Pr Me CF₃ Cl C—F CH CH CH i-Pr Me CF₃ F CH CH CH CH i-Pr Me CF₃acetylene CH CH CH CH i-Pr Me CF₃ I CH CH CH CH i-Pr Me CF₃ SO₂Me C—ClCH CH CH i-Pr Cl CF₃ Cl C—F CH CH CH i-Pr Cl CF₃ F CH CH CH CH i-Pr ClCF₃ acetylene CH CH CH CH i-Pr Cl CF₃ I CH CH CH CH i-Pr Cl CF₃ SO₂MeC—Cl CH CH CH i-Pr Me Br Cl C—F CH CH CH i-Pr Me Br F CH CH CH CH i-PrMe Br acetylene CH CH CH CH i-Pr Me Br I CH CH CH CH i-Pr Me Br SO₂MeC—Cl CH CH CH i-Pr Cl Br Cl C—F CH CH CH i-Pr Cl Br F CH CH CH CH i-PrCl Br acetylene CH CH CH CH i-Pr Cl Br I CH CH CH CH i-Pr Cl Br SO₂MeC—Cl CH CH N i-Pr Me CF₃ Cl C—F CH CH N i-Pr Me CF₃ F CH CH CH N i-Pr MeCF₃ acetylene CH CH CH N i-Pr Me CF₃ I CH CH CH N i-Pr Me CF₃ SO₂Me C—ClCH CH N i-Pr Cl CF₃ Cl C—F CH CH N i-Pr Cl CF₃ F CH CH CH N i-Pr Cl CF₃acetylene CH CH CH N i-Pr Cl CF₃ I CH CH CH N i-Pr Cl CF₃ SO₂Me C—Cl CHCH N i-Pr Me Br Cl C—F CH CH N i-Pr Me Br F CH CH CH N i-Pr Me Bracetylene CH CH CH N i-Pr Me Br I CH CH CH N i-Pr Me Br SO₂Me C—Cl CH CHN i-Pr Cl Br Cl C—F CH CH N i-Pr Cl Br F CH CH CH N i-Pr Cl Br acetyleneCH CH CH N i-Pr Cl Br I CH CH CH N i-Pr Cl Br SO₂Me CH N CH N i-Pr MeCF₃ H CH N CH N i-Pr Me CF₃ Me CH N CH N i-Pr Me CF₃ Cl CH N CH N i-PrCl CF₃ H CH N CH N i-Pr Cl CF₃ Me CH N CH N i-Pr Cl CF₃ Cl CH N CH Ni-Pr Me CN H CH N CH N i-Pr Me CN Me CH N CH N i-Pr Me CN Cl CH N CH Ni-Pr Cl CN H CH N CH N i-Pr Cl CN Me CH N CH N i-Pr Cl CN Cl CH N CH Ni-Pr Me Br H CH N CH N i-Pr Me Br Me CH N CH N i-Pr Me Br Cl CH N CH Ni-Pr Cl Br H CH N CH N i-Pr Cl Br Me CH N CH N i-Pr Cl Br Cl CH N CH Nt-Bu Me CF₃ H CH N CH N t-Bu Me CF₃ Me CH N CH N t-Bu Me CF₃ Cl CH N CHN t-Bu Cl CF₃ H CH N CH N t-Bu Cl CF₃ Me CH N CH N t-Bu Cl CF₃ Cl CH NCH N t-Bu Me CN H CH N CH N t-Bu Me CN Me CH N CH N t-Bu Me CN Cl CH NCH N t-Bu Cl CN H CH N CH N t-Bu Cl CN Me CH N CH N t-Bu Cl CN Cl CH NCH N t-Bu Me Br H CH N CH N t-Bu Me Br Me CH N CH N t-Bu Me Br Cl CH NCH N t-Bu Cl Br H CH N CH N t-Bu Cl Br Me CH N CH N t-Bu Cl Br Cl CH CHN N i-Pr Me CF₃ H CH CH N N i-Pr Me CF₃ Me CH CH N N i-Pr Me CF₃ Cl CHCH N N i-Pr Cl CF₃ H CH CH N N i-Pr Cl CF₃ Me CH CH N N i-Pr Cl CF₃ ClCH CH N N i-Pr Me CN H CH CH N N i-Pr Me CN Me CH CH N N i-Pr Me CN ClCH CH N N i-Pr Cl CN H CH CH N N i-Pr Cl CN Me CH CH N N i-Pr Cl CN ClCH CH N N i-Pr Me Br H CH CH N N i-Pr Me Br Me CH CH N N i-Pr Me Br ClCH CH N N i-Pr Cl Br H CH CH N N i-Pr Cl Br Me CH CH N N i-Pr Cl Br ClCH CH N N i-Pr Me CF₃ H CH CH N N i-Pr Me CF₃ Me CH CH N N i-Pr Me CF₃Cl CH CH N N i-Pr Cl CF₃ H CH CH N N i-Pr Cl CF₃ Me CH CH N N i-Pr ClCF₃ Cl CH CH N N i-Pr Me CN H CH CH N N i-Pr Me CN Me CH CH N N i-Pr MeCN Cl CH CH N N i-Pr Cl CN H CH CH N N i-Pr Cl CN Me CH CH N N i-Pr ClCN Cl CH CH N N i-Pr Me Br H CH CH N N i-Pr Me Br Me CH CH N N i-Pr MeBr Cl CH CH N N i-Pr Cl Br H CH CH N N i-Pr Cl Br Me CH CH N N i-Pr ClBr Cl

[0346] TABLE 10

R³ R⁴ R⁷ R⁸ R⁹ R¹⁰ Me CF₃ i-Pr Me H H Me CF₃ i-Pr Me H Me Me CF₃ i-Pr MeCl H Me CF₃ i-Pr Me Cl Me Me CF₃ i-Pr Me Me Me Cl CF₃ i-Pr Me H H Cl CF₃i-Pr Me H Me Cl CF₃ i-Pr Me Cl H Cl CF₃ i-Pr Me Cl Me Cl CF₃ i-Pr Me MeMe Me CF₃ t-Bu Me H H Me CF₃ t-Bu Me H Me Me CF₃ t-Bu Me Cl H Me CF₃t-Bu Me Cl Me Me CF₃ t-Bu Me Me Me Cl CF₃ t-Bu Me H H Cl CF₃ t-Bu Me HMe Cl CF₃ t-Bu Me Cl H Cl CF₃ t-Bu Me Cl Me Cl CF₃ t-Bu Me Me Me

[0347] TABLE 11

R³ R⁴ R⁷ R⁸ R⁹ R¹⁰ Me CF₃ i-Pr Me H Me Me CF₃ i-Pr Me Me Me Me CF₃ i-PrCl H Me Me CF₃ i-Pr Cl Me Me Cl CF₃ i-Pr Me H Me Cl CF₃ i-Pr Me Me Me ClCF₃ i-Pr Cl H Me Cl CF₃ i-Pr Cl Me Me Me CF₃ t-Bu Me H Me Me CF₃ t-Bu MeMe Me Me CF₃ t-Bu Cl H Me Me CF₃ t-Bu Cl Me Me Cl CF₃ t-Bu Me H Me ClCF₃ t-Bu Me Me Me Cl CF₃ t-Bu Cl H Me Cl CF₃ t-Bu Cl Me Me

[0348] TABLE 12

W X Y Z R³ R⁴ R⁷ R⁸ CH CH CH CH Et Me CF₃ Cl CH CH CH CH i-Pr Me CF₃ ClCH CH CH CH t-Bu Me CF₃ Cl CH CH CH CH Et Me CF₃ Br CH CH CH CH i-Pr MeCF₃ Br CH CH CH CH t-Bu Me CF₃ Br CH CH CH CH Et Me CF₃ I CH CH CH CHi-Pr Me CF₃ I CH CH CH CH t-Bu Me CF₃ I CH CH CH CH Et Me CF₃ F CH CH CHCH i-Pr Me CF₃ F CH CH CH CH t-Bu Me CF₃ F CH CH CH CH Et Me CF₃ Me CHCH CH CH i-Pr Me CF₃ Me CH CH CH CH t-Bu Me CF₃ Me CH CH CH CH Et Me CF₃CF₃ CH CH CH CH i-Pr Me CF₃ CF₃ CH CH CH CH t-Bu Me CF₃ CF₃ CH CH CH CHEt Me CF₃ OMe CH CH CH CH i-Pr Me CF₃ OMe CH CH CH CH t-Bu Me CF₃ OMe CHCH CH CH Et Me CF₃ CN CH CH CH CH i-Pr Me CF₃ CN CH CH CH CH t-Bu Me CF₃CN CH CH CH CH Et Cl CF₃ Cl CH CH CH CH i-Pr Cl CF₃ Cl CH CH CH CH t-BuCl CF₃ Cl CH CH CH CH Et Cl CF₃ Br CH CH CH CH i-Pr Cl CF₃ Br CH CH CHCH t-Bu Cl CF₃ Br CH CH CH CH Et Cl CF₃ I CH CH CH CH i-Pr Cl CF₃ I CHCH CH CH t-Bu Cl CF₃ I CH CH CH CH Et Cl CF₃ F CH CH CH CH i-Pr Cl CF₃ FCH CH CH CH t-Bu Cl CF₃ F CH CH CH CH Et Cl CF₃ Me CH CH CH CH i-Pr ClCF₃ Me CH CH CH CH t-Bu Cl CF₃ Me CH CH CH CH Et Cl CF₃ CF₃ CH CH CH CHi-Pr Cl CF₃ CF₃ CH CH CH CH t-Bu Cl CF₃ CF₃ CH CH CH CH Et Cl CF₃ OMe CHCH CH CH i-Pr Cl CF₃ OMe CH CH CH CH t-Bu Cl CF₃ OMe CH CH CH CH Et ClCF₃ CN CH CH CH CH i-Pr Cl CF₃ CN CH CH CH CH t-Bu Cl CF₃ CN CH CH CH NEt Me CF₃ Cl CH CH CH N i-Pr Me CF₃ Cl CH CH CH N t-Bu Me CF₃ Cl CH CHCH N Et Me CF₃ Br CH CH CH N i-Pr Me CF₃ Br CH CH CH N t-Bu Me CF₃ Br CHCH CH N Et Me CF₃ I CH CH CH N i-Pr Me CF₃ I CH CH CH N t-Bu Me CF₃ I CHCH CH N Et Me CF₃ F CH CH CH N i-Pr Me CF₃ F CH CH CH N t-Bu Me CF₃ F CHCH CH N Et Me CF₃ Me CH CH CH N i-Pr Me CF₃ Me CH CH CH N t-Bu Me CF₃ MeCH CH CH N Et Me CF₃ CF₃ CH CH CH N i-Pr Me CF₃ CF₃ CH CH CH N t-Bu MeCF₃ CF₃ CH CH CH N Et Me CF₃ OMe CH CH CH N i-Pr Me CF₃ OMe CH CH CH Nt-Bu Me CF₃ OMe CH CH CH N Et Me CF₃ CN CH CH CH N i-Pr Me CF₃ CN CH CHCH N t-Bu Me CF₃ CN CH CH CH N Et Cl CF₃ Cl CH CH CH N i-Pr Cl CF₃ Cl CHCH CH N t-Bu Cl CF₃ Cl CH CH CH N Et Cl CF₃ Br CH CH CH N i-Pr Cl CF₃ BrCH CH CH N t-Bu Cl CF₃ Br CH CH CH N Et Cl CF₃ I CH CH CH N i-Pr Cl CF₃I CH CH CH N t-Bu Cl CF₃ I CH CH CH N Et Cl CF₃ F CH CH CH N i-Pr Cl CF₃F CH CH CH N t-Bu Cl CF₃ F CH CH CH N Et Cl CF₃ Me CH CH CH N i-Pr ClCF₃ Me CH CH CH N t-Bu Cl CF₃ Me CH CH CH N Et Cl CF₃ CF₃ CH CH CH Ni-Pr Cl CF₃ CF₃ CH CH CH N t-Bu Cl CF₃ CF₃ CH CH CH N Et Cl CF₃ OMe CHCH CH N i-Pr Cl CF₃ OMe CH CH CH N t-Bu Cl CF₃ OMe CH CH CH N Et Cl CF₃CN CH CH CH N i-Pr Cl CF₃ CN CH CH CH N t-Bu Cl CF₃ CN CH CH N CH Et MeCF₃ Cl CH CH N CH i-Pr Me CF₃ Cl CH CH N CH t-Bu Me CF₃ Cl CH CH N CH EtMe CF₃ Br CH CH N CH i-Pr Me CF₃ Br CH CH N CH t-Bu Me CF₃ Br CH CH N CHEt Me CF₃ I CH CH N CH i-Pr Me CF₃ I CH CH N CH t-Bu Me CF₃ I CH CH N CHEt Me CF₃ F CH CH N CH i-Pr Me CF₃ F CH CH N CH t-Bu Me CF₃ F CH CH N CHEt Me CF₃ Me CH CH N CH i-Pr Me CF₃ Me CH CH N CH t-Bu Me CF₃ Me CH CH NCH Et Me CF₃ CF₃ CH CH N CH i-Pr Me CF₃ CF₃ CH CH N CH t-Bu Me CF₃ CF₃CH CH N CH Et Me CF₃ OMe CH CH N CH i-Pr Me CF₃ OMe CH CH N CH t-Bu MeCF₃ OMe CH CH N CH Et Me CF₃ CN CH CH N CH i-Pr Me CF₃ CN CH CH N CHt-Bu Me CF₃ CN CH CH N CH Et Cl CF₃ Cl CH CH N CH i-Pr Cl CF₃ Cl CH CH NCH t-Bu Cl CF₃ Cl CH CH N CH Et Cl CF₃ Br CH CH N CH i-Pr Cl CF₃ Br CHCH N CH t-Bu Cl CF₃ Br CH CH N CH Et Cl CF₃ I CH CH N CH i-Pr Cl CF₃ ICH CH N CH t-Bu Cl CF₃ I CH CH N CH Et Cl CF₃ F CH CH N CH i-Pr Cl CF₃ FCH CH N CH t-Bu Cl CF₃ F CH CH N CH Et Cl CF₃ Me CH CH N CH i-Pr Cl CF₃Me CH CH N CH t-Bu Cl CF₃ Me CH CH N CH Et Cl CF₃ CF₃ CH CH N CH i-Pr ClCF₃ CF₃ CH CH N CH t-Bu Cl CF₃ CF₃ CH CH N CH Et Cl CF₃ OMe CH CH N CHi-Pr Cl CF₃ OMe CH CH N CH t-Bu Cl CF₃ OMe CH CH N CH Et Cl CF₃ CN CH CHN CH i-Pr Cl CF₃ CN CH CH N CH t-Bu Cl CF₃ CN CH N CH CH Et Me CF₃ Cl CHN CH CH i-Pr Me CF₃ Cl CH N CH CH t-Bu Me CF₃ Cl CH N CH CH Et Me CF₃ BrCH N CH CH i-Pr Me CF₃ Br CH N CH CH t-Bu Me CF₃ Br CH N CH CH Et Me CF₃I CH N CH CH i-Pr Me CF₃ I CH N CH CH t-Bu Me CF₃ I CH N CH CH Et Me CF₃F CH N CH CH i-Pr Me CF₃ F CH N CH CH t-Bu Me CF₃ F CH N CH CH Et Me CF₃Me CH N CH CH i-Pr Me CF₃ Me CH N CH CH t-Bu Me CF₃ Me CH N CH CH Et MeCF₃ CF₃ CH N CH CH i-Pr Me CF₃ CF₃ CH N CH CH t-Bu Me CF₃ CF₃ CH N CH CHEt Me CF₃ OMe CH N CH CH i-Pr Me CF₃ OMe CH N CH CH t-Bu Me CF₃ OMe CH NCH CH Et Me CF₃ CN CH N CH CH i-Pr Me CF₃ CN CH N CH CH t-Bu Me CF₃ CNCH N CH CH Et Cl CF₃ Cl CH N CH CH i-Pr Cl CF₃ Cl CH N CH CH t-Bu Cl CF₃Cl CH N CH CH Et Cl CF₃ Br CH N CH CH i-Pr Cl CF₃ Br CH N CH CH t-Bu ClCF₃ Br CH N CH CH Et Cl CF₃ I CH N CH CH i-Pr Cl CF₃ I CH N CH CH t-BuCl CF₃ I CH N CH CH Et Cl CF₃ F CH N CH CH i-Pr Cl CF₃ F CH N CH CH t-BuCl CF₃ F CH N CH CH Et Cl CF₃ Me CH N CH CH i-Pr Cl CF₃ Me CH N CH CHt-Bu Cl CF₃ Me CH N CH CH Et Cl CF₃ CF₃ CH N CH CH i-Pr Cl CF₃ CF₃ CH NCH CH t-Bu Cl CF₃ CF₃ CH N CH CH Et Cl CF₃ OMe CH N CH CH i-Pr Cl CF₃OMe CH N CH CH t-Bu Cl CF₃ OMe CH N CH CH Et Cl CF₃ CN CH N CH CH i-PrCl CF₃ CN CH N CH CH t-Bu Cl CF₃ CN N CH CH CH Et Me CF₃ Cl N CH CH CHi-Pr Me CF₃ Cl N CH CH CH t-Bu Me CF₃ Cl N CH CH CH Et Me CF₃ Br N CH CHCH i-Pr Me CF₃ Br N CH CH CH t-Bu Me CF₃ Br N CH CH CH Et Me CF₃ I N CHCH CH i-Pr Me CF₃ I N CH CH CH t-Bu Me CF₃ I N CH CH CH Et Me CF₃ F N CHCH CH i-Pr Me CF₃ F N CH CH CH t-Bu Me CF₃ F N CH CH CH Et Me CF₃ Me NCH CH CH i-Pr Me CF₃ Me N CH CH CH t-Bu Me CF₃ Me N CH CH CH Et Me CF₃CF₃ N CH CH CH i-Pr Me CF₃ CF₃ N CH CH CH t-Bu Me CF₃ CF₃ N CH CH CH EtMe CF₃ OMe N CH CH CH i-Pr Me CF₃ OMe N CH CH CH t-Bu Me CF₃ OMe N CH CHCH Et Me CF₃ CN N CH CH CH i-Pr Me CF₃ CN N CH CH CH t-Bu Me CF₃ CN N CHCH CH Et Cl CF₃ Cl N CH CH CH i-Pr Cl CF₃ Cl N CH CH CH t-Bu Cl CF₃ Cl NCH CH CH Et Cl CF₃ Br N CH CH CH i-Pr Cl CF₃ Br N CH CH CH t-Bu Cl CF₃Br N CH CH CH Et Cl CF₃ I N CH CH CH i-Pr Cl CF₃ I N CH CH CH t-Bu ClCF₃ I N CH CH CH Et Cl CF₃ F N CH CH CH i-Pr Cl CF₃ F N CH CH CH t-Bu ClCF₃ F N CH CH CH Et Cl CF₃ Me N CH CH CH i-Pr Cl CF₃ Me N CH CH CH t-BuCl CF₃ Me N CH CH CH Et Cl CF₃ CF₃ N CH CH CH i-Pr Cl CF₃ CF₃ N CH CH CHt-Bu Cl CF₃ CF₃ N CH CH CH Et Cl CF₃ OMe N CH CH CH i-Pr Cl CF₃ OMe N CHCH CH t-Bu Cl CF₃ OMe N CH CH CH Et Cl CF₃ CN N CH CH CH i-Pr Cl CF₃ CNN CH CH CH t-Bu Cl CF₃ CN CH N CH N Et Me CF₃ Cl CH N CH N i-Pr Me CF₃Cl CH N CH N t-Bu Me CF₃ Cl CH N CH N Et Me CF₃ Br CH N CH N i-Pr Me CF₃Br CH N CH N t-Bu Me CF₃ Br CH N CH N Et Me CF₃ I CH N CH N i-Pr Me CF₃I CH N CH N t-Bu Me CF₃ I CH N CH N Et Me CF₃ F CH N CH N i-Pr Me CF₃ FCH N CH N t-Bu Me CF₃ F CH N CH N Et Me CF₃ Me CH N CH N i-Pr Me CF₃ MeCH N CH N t-Bu Me CF₃ Me CH N CH N Et Me CF₃ CF₃ CH N CH N i-Pr Me CF₃CF₃ CH N CH N t-Bu Me CF₃ CF₃ CH N CH N Et Me CF₃ OMe CH N CH N i-Pr MeCF₃ OMe CH N CH N t-Bu Me CF₃ OMe CH N CH N Et Me CF₃ CN CH N CH N i-PrMe CF₃ CN CH N CH N t-Bu Me CF₃ CN CH N CH N Et Cl CF₃ Cl CH N CH N i-PrCl CF₃ Cl CH N CH N t-Bu Cl CF₃ Cl CH N CH N Et Cl CF₃ Br CH N CH N i-PrCl CF₃ Br CH N CH N t-Bu Cl CF₃ Br CH N CH N Et Cl CF₃ I CH N CH N i-PrCl CF₃ I CH N CH N t-Bu Cl CF₃ I CH N CH N Et Cl CF₃ F CH N CH N i-Pr ClCF₃ F CH N CH N t-Bu Cl CF₃ F CH N CH N Et Cl CF₃ Me CH N CH N i-Pr ClCF₃ Me CH N CH N t-Bu Cl CF₃ Me CH N CH N Et Cl CF₃ CF₃ CH N CH N i-PrCl CF₃ CF₃ CH N CH N t-Bu Cl CF₃ CF₃ CH N CH N Et Cl CF₃ OMe CH N CH Ni-Pr Cl CF₃ OMe CH N CH N t-Bu Cl CF₃ OMe CH N CH N Et Cl CF₃ CN CH N CHN i-Pr Cl CF₃ CN CH N CH N t-Bu Cl CF₃ CN CH CH CH CCl Et Me CF₃ Cl CHCH CH CCl i-Pr Me CF₃ Cl CH CH CH CCl t-Bu Me CF₃ Cl CH CH CH CCl Et MeCF₃ Br CH CH CH CCl i-Pr Me CF₃ Br CH CH CH CCl t-Bu Me CF₃ Br CH CH CHCCl Et Me CF₃ I CH CH CH CCl i-Pr Me CF₃ I CH CH CH CCl t-Bu Me CF₃ I CHCH CH CCl Et Me CF₃ F CH CH CH CCl i-Pr Me CF₃ F CH CH CH CCl t-Bu MeCF₃ F CH CH CH CCl Et Me CF₃ Me CH CH CH CCl i-Pr Me CF₃ Me CH CH CH CClt-Bu Me CF₃ Me CH CH CH CCl Et Me CF₃ CF₃ CH CH CH CCl i-Pr Me CF₃ CF₃CH CH CH CCl t-Bu Me CF₃ CF₃ CH CH CH CCl Et Me CF₃ OMe CH CH CH CCli-Pr Me CF₃ OMe CH CH CH CCl t-Bu Me CF₃ OMe CH CH CH CCl Et Me CF₃ CNCH CH CH CCl i-Pr Me CF₃ CN CH CH CH CCl t-Bu Me CF₃ CN CH CH CH CCl EtCl CF₃ Cl CH CH CH CCl i-Pr Cl CF₃ Cl CH CH CH CCl t-Bu Cl CF₃ Cl CH CHCH CCl Et Cl CF₃ Br CH CH CH CCl i-Pr Cl CF₃ Br CH CH CH CCl t-Bu Cl CF₃Br CH CH CH CCl Et Cl CF₃ I CH CH CH CCl i-Pr Cl CF₃ I CH CH CH CCl t-BuCl CF₃ I CH CH CH CCl Et Cl CF₃ F CH CH CH CCl i-Pr Cl CF₃ F CH CH CHCCl t-Bu Cl CF₃ F CH CH CH CCl Et Cl CF₃ Me CH CH CH CCl i-Pr Cl CF₃ MeCH CH CH CCl t-Bu Cl CF₃ Me CH CH CH CCl Et Cl CF₃ CF₃ CH CH CH CCl i-PrCl CF₃ CF₃ CH CH CH CCl t-Bu Cl CF₃ CF₃ CH CH CH CCl Et Cl CF₃ OMe CH CHCH CCl i-Pr Cl CF₃ OMe CH CH CH CCl t-Bu Cl CF₃ OMe CH CH CH CCl Et ClCF₃ CN CH CH CH CCl i-Pr Cl CF₃ CN CH CH CH CCl t-Bu Cl CF₃ CN CH CH CHCF Et Me CF₃ Cl CH CH CH CF i-Pr Me CF₃ Cl CH CH CH CF t-Bu Me CF₃ Cl CHCH CH CF Et Me CF₃ Br CH CH CH CF i-Pr Me CF₃ Br CH CH CH CF t-Bu Me CF₃Br CH CH CH CF Et Me CF₃ I CH CH CH CF i-Pr Me CF₃ I CH CH CH CF t-Bu MeCF₃ I CH CH CH CF Et Me CF₃ F CH CH CH CF i-Pr Me CF₃ F CH CH CH CF t-BuMe CF₃ F CH CH CH CF Et Me CF₃ Me CH CH CH CF i-Pr Me CF₃ Me CH CH CH CFt-Bu Me CF₃ Me CH CH CH CF Et Me CF₃ CF₃ CH CH CH CF i-Pr Me CF₃ CF₃ CHCH CH CF t-Bu Me CF₃ CF₃ CH CH CH CF Et Me CF₃ OMe CH CH CH CF i-Pr MeCF₃ OMe CH CH CH CF t-Bu Me CF₃ OMe CH CH CH CF Et Me CF₃ CN CH CH CH CFi-Pr Me CF₃ CN CH CH CH CF t-Bu Me CF₃ CN CH CH CH CF Et Cl CF₃ Cl CH CHCH CF i-Pr Cl CF₃ Cl CH CH CH CF t-Bu Cl CF₃ Cl CH CH CH CF Et Cl CF₃ BrCH CH CH CF i-Pr Cl CF₃ Br CH CH CH CF t-Bu Cl CF₃ Br CH CH CH CF Et ClCF₃ I CH CH CH CF i-Pr Cl CF₃ I CH CH CH CF t-Bu Cl CF₃ I CH CH CH CFi-Pr Cl CF₃ F CH CH CH CF t-Bu Cl CF₃ F CH CH CH CF Et Cl CF₃ Me CH CHCH CF i-Pr Cl CF₃ Me CH CH CH CF t-Bu Cl CF₃ Me CH CH CH CF Et Cl CF₃CF₃ CH CH CH CF i-Pr Cl CF₃ CF₃ CH CH CH CF t-Bu Cl CF₃ CF₃ CH CH CH CFEt Cl CF₃ OMe CH CH CH CF i-Pr Cl CF₃ OMe CH CH CH CF t-Bu Cl CF₃ OMe CHCH CH CF Et Cl CF₃ CN CH CH CH CF i-Pr Cl CF₃ CN CH CH CH CF t-Bu Cl CF₃CN CH CH CH CH Et Me C₂F₅ Cl CH CH CH CH i-Pr Me C₂F₅ Cl CH CH CH CHt-Bu Me C₂F₅ Cl CH CH CH CH Et Me C₂F₅ Br CH CH CH CH i-Pr Me C₂F₅ Br CHCH CH CH t-Bu Me C₂F₅ Br CH CH CH CH Et Me C₂F₅ I CH CH CH CH i-Pr MeC₂F₅ I CH CH CH CH t-Bu Me C₂F₅ I CH CH CH CH Et Me C₂F₅ F CH CH CH CHi-Pr Me C₂F₅ F CH CH CH CH t-Bu Me C₂F₅ F CH CH CH CH Et Me C₂F₅ Me CHCH CH CH i-Pr Me C₂F₅ Me CH CH CH CH t-Bu Me C₂F₅ Me CH CH CH CH Et MeC₂F₅ CF₃ CH CH CH CH i-Pr Me C₂F₅ CF₃ CH CH CH CH t-Bu Me C₂F₅ CF₃ CH CHCH CH Et Me C₂F₅ OMe CH CH CH CH i-Pr Me C₂F₅ OMe CH CH CH CH t-Bu MeC₂F₅ OMe CH CH CH CH Et Me C₂F₅ CN CH CH CH CH i-Pr Me C₂F₅ CN CH CH CHCH t-Bu Me C₂F₅ CN CH CH CH CH Et Cl C₂F₅ Cl CH CH CH CH i-Pr Cl C₂F₅ ClCH CH CH CH t-Bu Cl C₂F₅ Cl CH CH CH CH Et Cl C₂F₅ Br CH CH CH CH i-PrCl C₂F₅ Br CH CH CH CH t-Bu Cl C₂F₅ Br CH CH CH CH Et Cl C₂F₅ I CH CH CHCH i-Pr Cl C₂F₅ I CH CH CH CH t-Bu Cl C₂F₅ I CH CH CH CH Et Cl C₂F₅ F CHCH CH CH i-Pr Cl C₂F₅ F CH CH CH CH t-Bu Cl C₂F₅ F CH CH CH CH Et ClC₂F₅ Me CH CH CH CH i-Pr Cl C₂F₅ Me CH CH CH CH t-Bu Cl C₂F₅ Me CH CH CHCH Et Cl C₂F₅ CF₃ CH CH CH CH i-Pr Cl C₂F₅ CF₃ CH CH CH CH t-Bu Cl C₂F₅CF₃ CH CH CH CH Et Cl C₂F₅ OMe CH CH CH CH i-Pr Cl C₂F₅ OMe CH CH CH CHt-Bu Cl C₂F₅ OMe CH CH CH CH Et Cl C₂F₅ CN CH CH CH CH i-Pr Cl C₂F₅ CNCH CH CH CH t-Bu Cl C₂F₅ CN

[0349] TABLE 13

W X Y Z R³ R⁴ R⁷ R⁸ CH CH CH CH Et Me CF₃ Cl CH CH CH CH i-Pr Me CF₃ ClCH CH CH CH t-Bu Me CF₃ Cl CH CH CH CH Et Me CF₃ Br CH CH CH CH i-Pr MeCF₃ Br CH CH CH CH i-Bu Me CF₃ Br CH CH CH CH Et Me CF₃ I CH CH CH CHi-Pr Me CF₃ I CH CH CH CH t-Bu Me CF₃ I CH CH CH CH Et Me CF₃ F CH CH CHCH i-Pr Me CF₃ F CH CH CH CH t-Bu Me CF₃ F CH CH CH CH Et Me CF₃ Me CHCH CH CH i-Pr Me CF₃ Me CH CH CH CH t-Bu Me CF₃ Me CH CH CH CH Et Me CF₃CF₃ CH CH CH CH i-Pr Me CF₃ CF₃ CH CH CH CH t-Bu Me CF₃ CF₃ CH CH CH CHEt Me CF₃ OMe CH CH CH CH i-Pr Me CF₃ OMe CH CH CH CH t-Bu Me CF₃ OMe CHCH CH CH Et Me CF₃ CN CH CH CH CH i-Pr Me CF₃ CN CH CH CH CH t-Bu Me CF₃CN CH CH CH CH Et Cl CF₃ Cl CH CH CH CH i-Pr Cl CF₃ Cl CH CH CH CH t-BuCl CF₃ Cl CH CH CH CH Et Cl CF₃ Br CH CH CH CH i-Pr Cl CF₃ Br CH CH CHCH t-Bu Cl CF₃ Br CH CH CH CH Et Cl CF₃ I CH CH CH CH i-Pr Cl CF₃ I CHCH CH CH t-Bu Cl CF₃ I CH CH CH CH Et Cl CF₃ F CH CH CH CH i-Pr Cl CF₃ FCH CH CH CH t-Bu Cl CF₃ F CH CH CH CH Et Cl CF₃ Me CH CH CH CH i-Pr ClCF₃ Me CH CH CH CH t-Bu Cl CF₃ Me CH CH CH CH Et Cl CF₃ CF₃ CH CH CH CHi-Pr Cl CF₃ CF₃ CH CH CH CH t-Bu Cl CF₃ CF₃ CH CH CH CH Et Cl CF₃ OMe CHCH CH CH i-Pr CI CF₃ OMe CH CH CH CH t-Bu Cl CF₃ OMe CH CH CH CH Et ClCF₃ CN CH CH CH CH i-Pr Cl CF₃ CN CH CH CH CH t-Bu Cl CF₃ CN CH CH CH NEt Me CF₃ Cl CH CH CH N i-Pr Me CF₃ Cl CH CH CH N t-Bu Me CF₃ Cl CH CHCH N Et Me CF₃ Br CH CH CH N i-Pr Me CF₃ Br CH CH CH N t-Bu Me CF₃ Br CHCH CH N Et Me CF₃ I CH CH CH N i-Pr Me CF₃ I CH CH CH N t-Bu Me CF₃ I CHCH CH N Et Me CF₃ F CH CH CH N i-Pr Me CF₃ F CH CH CH N t-Bu Me CF₃ F CHCH CH N Et Me CF₃ Me CH CH CH N i-Pr Me CF₃ Me CH CH CH N t-Bu Me CF₃ MeCH CH CH N Et Me CF₃ CF₃ CH CH CH N i-Pr Me CF₃ CF₃ CH CH CH N t-Bu MeCF₃ CF₃ CH CH CH N Et Me CF₃ OMe CH CH CH N i-Pr Me CF₃ OMe CH CH CH Nt-Bu Me CF₃ OMe CH CH CH N Et Me CF₃ CN CH CH CH N i-Pr Me CF₃ CN CH CHCH N t-Bu Me CF₃ CN CH CH CH N Et Cl CF₃ Cl CH CH CH N i-Pr Cl CF₃ Cl CHCH CH N t-Bu Cl CF₃ Cl CH CH CH N Et Cl CF₃ Br CH CH CH N i-Pr Cl CF₃ BrCH CH CH N t-Bu Cl CF₃ Br CH CH CH N Et Cl CF₃ I CH CH CH N i-Pr Cl CF₃I CH CH CH N t-Bu Cl CF₃ I CH CH CH N Et Cl CF₃ F CH CH CH N i-Pr Cl CF₃F CH CH CH N t-Bu Cl CF₃ F CH CH CH N Et Cl CF₃ Me CH CH CH N i-Pr ClCF₃ Me CH CH CH N t-Bu Cl CF₃ Me CH CH CH N Et Cl CF₃ CF₃ CH CH CH Ni-Pr Cl CF₃ CF₃ CH CH CH N t-Bu Cl CF₃ CF₃ CH CH CH N Et Cl CF₃ OMe CHCH CH N i-Pr Cl CF₃ OMe CH CH CH N t-Bu Cl CF₃ OMe CH CH CH N Et Cl CF₃CN CH CH CH N i-Pr Cl CF₃ CN CH CH CH N t-Bu Cl CF₃ CN CH CH N CH Et MeCF₃ Cl CH CH N CH i-Pr Me CF₃ Cl CH CH N CH t-Bu Me CF₃ Cl CH CH N CH EtMe CF₃ Br CH CH N CH i-Pr Me CF₃ Br CH CH N CH t-Bu Me CF₃ Br CH CH N CHEt Me CF₃ I CH CH N CH i-Pr Me CF₃ I CH CH N CH t-Bu Me CF₃ I CH CH N CHEt Me CF₃ F CH CH N CH i-Pr Me CF₃ F CH CH N CH t-Bu Me CF₃ F CH CH N CHEt Me CF₃ Me CH CH N CH i-Pr Me CF₃ Me CH CH N CH t-Bu Me CF₃ Me CH CH NCH Et Me CF₃ CF₃ CH CH N CH i-Pr Me CF₃ CF₃ CH CH N CH t-Bu Me CF₃ CF₃CH CH N CH Et Me CF₃ OMe CH CH N CH i-Pr Me CF₃ OMe CH CH N CH t-Bu MeCF₃ OMe CH CH N CH Et Me CF₃ CN CH CH N CH i-Pr Me CF₃ CN CH CH N CHt-Bu Me CF₃ CN CH CH N CH Et Cl CF₃ Cl CH CH N CH i-Pr Cl CF₃ Cl CH CH NCH t-Bu Cl CF₃ Cl CH CH N CH Et Cl CF₃ Br CH CH N CH i-Pr Cl CF₃ Br CHCH N CH t-Bu Cl CF₃ Br CH CH N CH Et Cl CF₃ I CH CH N CH i-Pr Cl CF₃ ICH CH N CH t-Bu Cl CF₃ I CH CH N CH Et Cl CF₃ F CH CH N CH i-Pr Cl CF₃ FCH CH N CH t-Bu Cl CF₃ F CH CH N CH Et Cl CF₃ Me CH CH N CH i-Pr Cl CF₃Me CH CH N CH t-Bu Cl CF₃ Me CH CH N CH Et Cl CF₃ CF₃ CH CH N CH i-Pr ClCF₃ CF₃ CH CH N CH t-Bu Cl CF₃ CF₃ CH CH N CH Et Cl CF₃ OMe CH CH N CHi-Pr Cl CF₃ OMe CH CH N CH t-Bu Cl CF₃ OMe CH CH N CH Et Cl CF₃ CN CH CHN CH i-Pr Cl CF₃ CN CH CH N CH t-Bu Cl CF₃ CN CH N CH CH Et Me CF₃ Cl CHN CH CH i-Pr Me CF₃ Cl CH N CH CH t-Bu Me CF₃ Cl CH N CH CH Et Me CF₃ BrCH N CH CH i-Pr Me CF₃ Br CH N CH CH t-Bu Me CF₃ Br CH N CH CH Et Me CF₃I CH N CH CH i-Pr Me CF₃ I CH N CH CH t-Bu Me CF₃ I CH N CH CH Et Me CF₃F CH N CH CH i-Pr Me CF₃ F CH N CH CH t-Bu Me CF₃ F CH N CH CH Et Me CF₃Me CH N CH CH i-Pr Me CF₃ Me CH N CH CH t-Bu Me CF₃ Me CH N CH CH Et MeCF₃ CF₃ CH N CH CH i-Pr Me CF₃ CF₃ CH N CH CH t-Bu Me CF₃ CF₃ CH N CH CHEt Me CF₃ OMe CH N CH CH i-Pr Me CF₃ OMe CH N CH CH t-Bu Me CF₃ OMe CH NCH CH Et Me CF₃ CN CH N CH CH i-Pr Me CF₃ CN CH N CH CH t-Bu Me CF₃ CNCH N CH CH Et Cl CF₃ Cl CH N CH CH i-Pr Cl CF₃ Cl CH N CH CH t-Bu Cl CF₃Cl CH N CH CH Et Cl CF₃ Br CH N CH CH i-Pr Cl CF₃ Br CH N CH CH t-Bu ClCF₃ Br CH N CH CH Et Cl CF₃ I CH N CH CH i-Pr Cl CF₃ I CH N CH CH t-BuCl CF₃ I CH N CH CH Et Cl CF₃ F CH N CH CH i-Pr Cl CF₃ F CH N CH CH t-BuCl CF₃ F CH N CH CH Et Cl CF₃ Me CH N CH CH i-Pr Cl CF₃ Me CH N CH CHt-Bu Cl CF₃ Me CH N CH CH Et Cl CF₃ CF₃ CH N CH CH i-Pr Cl CF₃ CF₃ CH NCH CH t-Bu Cl CF₃ CF₃ CH N CH CH Et Cl CF₃ OMe CH N CH CH i-Pr Cl CF₃OMe CH N CH CH t-Bu Cl CF₃ OMe CH N CH CH Et Cl CF₃ CN CH N CH CH i-PrCl CF₃ CN CH N CH CH t-Bu Cl CF₃ CN N CH CH CH Et Me CF₃ Cl N CH CH CHi-Pr Me CF₃ Cl N CH CH CH t-Bu Me CF₃ Cl N CH CH CH Et Me CF₃ Br N CH CHCH i-Pr Me CF₃ Br N CH CH CH t-Bu Me CF₃ Br N CH CH CH Et Me CF₃ I N CHCH CH i-Pr Me CF₃ I N CH CH CH t-Bu Me CF₃ I N CH CH CH Et Me CF₃ F N CHCH CH i-Pr Me CF₃ F N CH CH CH t-Bu Me CF₃ F N CH CH CH Et Me CF₃ Me NCH CH CH i-Pr Me CF₃ Me N CH CH CH t-Bu Me CF₃ Me N CH CH CH Et Me CF₃CF₃ N CH CH CH i-Pr Me CF₃ CF₃ N CH CH CH t-Bu Me CF₃ CF₃ N CH CH CH EtMe CF₃ OMe N CH CH CH i-Pr Me CF₃ OMe N CH CH CH t-Bu Me CF₃ OMe N CH CHCH Et Me CF₃ CN N CH CH CH i-Pr Me CF₃ CN N CH CH CH t-Bu Me CF₃ CN N CHCH CH Et Cl CF₃ Cl N CH CH CH i-Pr Cl CF₃ Cl N CH CH CH t-Bu Cl CF₃ Cl NCH CH CH Et Cl CF₃ Br N CH CH CH i-Pr Cl CF₃ Br N CH CH CH t-Bu Cl CF₃Br N CH CH CH Et Cl CF₃ I N CH CH CH i-Pr Cl CF₃ I N CH CH CH t-Bu ClCF₃ I N CH CH CH Et Cl CF₃ F N CH CH CH i-Pr Cl CF₃ F N CH CH CH t-Bu ClCF₃ F N CH CH CH Et Cl CF₃ Me N CH CH CH i-Pr Cl CF₃ Me N CH CH CH t-BuCl CF₃ Me N CH CH CH Et Cl CF₃ CF₃ N CH CH CH i-Pr Cl CF₃ CF₃ N CH CH CHt-Bu Cl CF₃ CF₃ N CH CH CH Et Cl CF₃ OMe N CH CH CH i-Pr Cl CF₃ OMe N CHCH CH t-Bu Cl CF₃ OMe N CH CH CH Et Cl CF₃ CN N CH CH CH i-Pr Cl CF₃ CNN CH CH CH t-Bu Cl CF₃ CN CH N CH N Et Me CF₃ Cl CH N CH N i-Pr Me CF₃Cl CH N CH N t-Bu Me CF₃ Cl CH N CH N Et Me CF₃ Br CH N CH N i-Pr Me CF₃Br CH N CH N t-Bu Me CF₃ Br CH N CH N Et Me CF₃ I CH N CH N i-Pr Me CF₃I CH N CH N t-Bu Me CF₃ I CH N CH N Et Me CF₃ F CH N CH N i-Pr Me CF₃ FCH N CH N t-Bu Me CF₃ F CH N CH N Et Me CF₃ Me CH N CH N i-Pr Me CF₃ MeCH N CH N t-Bu Me CF₃ Me CH N CH N Et Me CF₃ CF₃ CH N CH N i-Pr Me CF₃CF₃ CH N CH N t-Bu Me CF₃ CF₃ CH N CH N Et Me CF₃ OMe CH N CH N i-Pr MeCF₃ OMe CH N CH N t-Bu Me CF₃ OMe CH N CH N Et Me CF₃ CN CH N CH N i-PrMe CF₃ CN CH N CH N t-Bu Me CF₃ CN CH N CH N Et Cl CF₃ Cl CH N CH N i-PrCl CF₃ Cl CH N CH N t-Bu Cl CF₃ Cl CH N CH N Et Cl CF₃ Br CH N CH N i-PrCl CF₃ Br CH N CH N t-Bu Cl CF₃ Br CH N CH N Et Cl CF₃ I CH N CH N i-PrCl CF₃ I CH N CH N t-Bu Cl CF₃ I CH N CH N Et Cl CF₃ F CH N CH N i-Pr ClCF₃ F CH N CH N t-Bu Cl CF₃ F CH N CH N Et Cl CF₃ Me CH N CH N i-Pr ClCF₃ Me CH N CH N t-Bu Cl CF₃ Me CH N CH N Et Cl CF₃ CF₃ CH N CH N i-PrCl CF₃ CF₃ CH N CH N t-Bu Cl CF₃ CF₃ CH N CH N Et Cl CF₃ OMe CH N CH Ni-Pr Cl CF₃ OMe CH N CH N t-Bu Cl CF₃ OMe CH N CH N Et Cl CF₃ CN CH N CHN i-Pr Cl CF₃ CN CH N CH N t-Bu Cl CF₃ CN CH CH CH CCl Et Me CF₃ Cl CHCH CH CCl i-Pr Me CF₃ Cl CH CH CH CCl t-Bu Me CF₃ Cl CH CH CH CCl Et MeCF₃ Br CH CH CH CCl i-Pr Me CF₃ Br CH CH CH CCl t-Bu Me CF₃ Br CH CH CHCCl Et Me CF₃ I CH CH CH CCl i-Pr Me CF₃ I CH CH CH CCl t-Bu Me CF₃ I CHCH CH CCl Et Me CF₃ F CH CH CH CCl i-Pr Me CF₃ F CH CH CH CCl t-Bu MeCF₃ F CH CH CH CCl Et Me CF₃ Me CH CH CH CCl i-Pr Me CF₃ Me CH CH CH CClt-Bu Me CF₃ Me CH CH CH CCl Et Me CF₃ CF₃ CH CH CH CCl i-Pr Me CF₃ CF₃CH CH CH CCl t-Bu Me CF₃ CF₃ CH CH CH CCl Et Me CF₃ OMe CH CH CH CCli-Pr Me CF₃ OMe CH CH CH CCl t-Bu Me CF₃ OMe CH CH CH CCl Et Me CF₃ CNCH CH CH CCl i-Pr Me CF₃ CN CH CH CH CCl t-Bu Me CF₃ CN CH CH CH CCl EtCl CF₃ Cl CH CH CH CCl i-Pr Cl CF₃ Cl CH CH CH CCl t-Bu Cl CF₃ Cl CH CHCH CCl Et Cl CF₃ Br CH CH CH CCl i-Pr Cl CF₃ Br CH CH CH CCl i-Bu Cl CF₃Br CH CH CH CCl Et Cl CF₃ I CH CH CH CCl i-Pr Cl CF₃ I CH CH CH CCl t-BuCl CF₃ I CH CH CH CCl Et Cl CF₃ F CH CH CH CCl i-Pr Cl CF₃ F CH CH CHCCl t-Bu Cl CF₃ F CH CH CH CCl Et Cl CF₃ Me CH CH CH CCl i-Pr Cl CF₃ MeCH CH CH CCl t-Bu Cl CF₃ Me CH CH CH CCl Et Cl CF₃ CF₃ CH CH CH CCl i-PrCl CF₃ CF₃ CH CH CH CCl t-Bu Cl CF₃ CF₃ CH CH CH CCl Et Cl CF₃ OMe CH CHCH CCl i-Pr Cl CF₃ OMe CH CH CH CCl t-Bu Cl CF₃ OMe CH CH CH CCl Et ClCF₃ CN CH CH CH CCl i-Pr Cl CF₃ CN CH CH CH CCl t-Bu Cl CF₃ CN CH CH CHCF Et Me CF₃ Cl CH CH CH CF i-Pr Me CF₃ Cl CH CH CH CF t-Bu Me CF₃ Cl CHCH CH CF Et Me CF₃ Br CH CH CH CF i-Pr Me CF₃ Br CH CH CH CF t-Bu Me CF₃Br CH CH CH CF Et Me CF₃ I CH CH CH CF i-Pr Me CF₃ I CH CH CH CF t-Bu MeCF₃ I CH CH CH CF Et Me CF₃ F CH CH CH CF i-Pr Me CF₃ F CH CH CH CF t-BuMe CF₃ F CH CH CH CF Et Me CF₃ Me CH CH CH CF i-Pr Me CF₃ Me CH CH CH CFt-Bu Me CF₃ Me CH CH CH CF Et Me CF₃ CF₃ CH CH CH CF i-Pr Me CF₃ CF₃ CHCH CH CF t-Bu Me CF₃ CF₃ CH CH CH CF Et Me CF₃ OMe CH CH CH CF i-Pr MeCF₃ OMe CH CH CH CF t-Bu Me CF₃ OMe CH CH CH CF Et Me CF₃ CN CH CH CH CFi-Pr Me CF₃ CN CH CH CH CF t-Bu Me CF₃ CN CH CH CH CF Et Cl CF₃ Cl CH CHCH CF i-Pr Cl CF₃ Cl CH CH CH CF t-Bu Cl CF₃ Cl CH CH CH CF Et Cl CF₃ BrCH CH CH CF i-Pr Cl CF₃ Br CH CH CH CF t-Bu Cl CF₃ Br CH CH CH CF Et ClCF₃ I CH CH CH CF i-Pr Cl CF₃ I CH CH CH CF t-Bu Cl CF₃ I CH CH CH CFi-Pr Cl CF₃ F CH CH CH CF t-Bu Cl CF₃ F CH CH CH CF Et Cl CF₃ Me CH CHCH CF i-Pr Cl CF₃ Me CH CH CH CF t-Bu Cl CF₃ Me CH CH CH CF Et Cl CF₃CF₃ CH CH CH CF i-Pr CI CF₃ CF₃ CH CH CH CF t-Bu Cl CF₃ CF₃ CH CH CH CFEt Cl CF₃ OMe CH CH CH CF i-Pr Cl CF₃ OMe CH CH CH CF t-Bu Cl CF₃ OMe CHCH CH CF Et Cl CF₃ CN CH CH CH CF i-Pr Cl CF₃ CN CH CH CH CF t-Bu Cl CF₃CN CH CH CH CH Et Me C₂F₅ Cl CH CH CH CH i-Pr Me C₂F₅ Cl CH CH CH CHt-Bu Me C₂F₅ Cl CH CH CH CH Et Me C₂F₅ Br CH CH CH CH i-Pr Me C₂F₅ Br CHCH CH CH t-Bu Me C₂F₅ Br CH CH CH CH Et Me C₂F₅ I CH CH CH CH i-Pr MeC₂F₅ I CH CH CH CH t-Bu Me C₂F₅ I CH CH CH CH Et Me C₂F₅ F CH CH CH CHi-Pr Me C₂F₅ F CH CH CH CH t-Bu Me C₂F₅ F CH CH CH CH Et Me C₂F₅ Me CHCH CH CH i-Pr Me C₂F₅ Me CH CH CH CH t-Bu Me C₂F₅ Me CH CH CH CH Et MeC₂F₅ CF₃ CH CH CH CH i-Pr Me C₂F₅ CF₃ CH CH CH CH t-Bu Me C₂F₅ CF₃ CH CHCH CH Et Me C₂F₅ OMe CH CH CH CH i-Pr Me C₂F₅ OMe CH CH CH CH t-Bu MeC₂F₅ OMe CH CH CH CH Et Me C₂F₅ CN CH CH CH CH i-Pr Me C₂F₅ CN CH CH CHCH t-Bu Me C₂F₅ CN CH CH CH CH Et Cl C₂F₅ Cl CH CH CH CH i-Pr Cl C₂F₅ ClCH CH CH CH t-Bu Cl C₂F₅ Cl CH CH CH CH Et Cl C₂F₅ Br CH CH CH CH i-PrCl C₂F₅ Br CH CH CH CH t-Bu Cl C₂F₅ Br CH CH CH CH Et Cl C₂F₅ I CH CH CHCH i-Pr Cl C₂F₅ I CH CH CH CH t-Bu Cl C₂F₅ I CH CH CH CH Et Cl C₂F₅ F CHCH CH CH i-Pr Cl C₂F₅ F CH CH CH CH t-Bu Cl C₂F₅ F CH CH CH CH Et ClC₂F₅ Me CH CH CH CH i-Pr Cl C₂F₅ Me CH CH CH CH t-Bu Cl C₂F₅ Me CH CH CHCH Et Cl C₂F₅ CF₃ CH CH CH CH i-Pr Cl C₂F₅ CF₃ CH CH CH CH t-Bu Cl C₂F₅CF₃ CH CH CH CH Et Cl C₂F₅ OMe CH CH CH CH i-Pr Cl C₂F₅ OMe CH CH CH CHt-Bu Cl C₂F₅ OMe CH CH CH CH Et Cl C₂F₅ CN CH CH CH CH i-Pr Cl C₂F₅ CNCH CH CH CH t-Bu Cl C₂F₅ CN

[0350] TABLE 14

W X Y Z R³ R⁴ R⁷ R⁸ CH CH CH CH Et Me CF₃ Cl CH CH CH CH i-Pr Me CF₃ ClCH CH CH CH t-Bu Me CF₃ Cl CH CH CH CH Et Me CF₃ Br CH CH CH CH i-Pr MeCF₃ Br CH CH CH CH t-Bu Me CF₃ Br CH CH CH CH Et Me CF₃ I CH CH CH CHi-Pr Me CF₃ I CH CH CH CH t-Bu Me CF₃ I CH CH CH CH Et Me CF₃ F CH CH CHCH i-Pr Me CF₃ F CH CH CH CH t-Bu Me CF₃ F CH CH CH CH Et Me CF₃ Me CHCH CH CH i-Pr Me CF₃ Me CH CH CH CH t-Bu Me CF₃ Me CH CH CH CH Et Me CF₃CF₃ CH CH CH CH i-Pr Me CF₃ CF₃ CH CH CH CH t-Bu Me CF₃ CF₃ CH CH CH CHEt Me CF₃ OMe CH CH CH CH i-Pr Me CF₃ OMe CH CH CH CH t-Bu Me CF₃ OMe CHCH CH CH Et Me CF₃ CN CH CH CH CH i-Pr Me CF₃ CN CH CH CH CH t-Bu Me CF₃CN CH CH CH CH Et Cl CF₃ Cl CH CH CH CH i-Pr Cl CF₃ Cl CH CH CH CH t-BuCl CF₃ Cl CH CH CH CH Et Cl CF₃ Br CH CH CH CH i-Pr Cl CF₃ Br CH CH CHCH t-Bu Cl CF₃ Br CH CH CH CH Et Cl CF₃ I CH CH CH CH i-Pr Cl CF₃ I CHCH CH CH t-Bu Cl CF₃ I CH CH CH CH Et Cl CF₃ F CH CH CH CH i-Pr Cl CF₃ FCH CH CH CH t-Bu Cl CF₃ F CH CH CH CH Et Cl CF₃ Me CH CH CH CH i-Pr ClCF₃ Me CH CH CH CH t-Bu Cl CF₃ Me CH CH CH CH Et Cl CF₃ CF₃ CH CH CH CHi-Pr Cl CF₃ CF₃ CH CH CH CH t-Bu Cl CF₃ CF₃ CH CH CH CH Et Cl CF₃ OMe CHCH CH CH i-Pr Cl CF₃ OMe CH CH CH CH t-Bu Cl CF₃ OMe CH CH CH CH Et ClCF₃ CN CH CH CH CH i-Pr Cl CF₃ CN CH CH CH CH t-Bu Cl CF₃ CN CH CH CH NEt Me CF₃ Cl CH CH CH N i-Pr Me CF₃ Cl CH CH CH N t-Bu Me CF₃ Cl CH CHCH N Et Me CF₃ Br CH CH CH N i-Pr Me CF₃ Br CH CH CH N t-Bu Me CF₃ Br CHCH CH N Et Me CF₃ I CH CH CH N i-Pr Me CF₃ I CH CH CH N t-Bu Me CF₃ I CHCH CH N Et Me CF₃ F CH CH CH N i-Pr Me CF₃ F CH CH CH N t-Bu Me CF₃ F CHCH CH N Et Me CF₃ Me CH CH CH N i-Pr Me CF₃ Me CH CH CH N t-Bu Me CF₃ MeCH CH CH N Et Me CF₃ CF₃ CH CH CH N i-Pr Me CF₃ CF₃ CH CH CH N t-Bu MeCF₃ CF₃ CH CH CH N Et Me CF₃ OMe CH CH CH N i-Pr Me CF₃ OMe CH CH CH Nt-Bu Me CF₃ OMe CH CH CH N Et Me CF₃ CN CH CH CH N i-Pr Me CF₃ CN CH CHCH N t-Bu Me CF₃ CN CH CH CH N Et Cl CF₃ Cl CH CH CH N i-Pr Cl CF₃ Cl CHCH CH N t-Bu Cl CF₃ Cl CH CH CH N Et Cl CF₃ Br CH CH CH N i-Pr Cl CF₃ BrCH CH CH N t-Bu Cl CF₃ Br CH CH CH N Et Cl CF₃ I CH CH CH N i-Pr Cl CF₃I CH CH CH N t-Bu Cl CF₃ I CH CH CH N Et Cl CF₃ F CH CH CH N i-Pr Cl CF₃F CH CH CH N t-Bu Cl CF₃ F CH CH CH N Et Cl CF₃ Me CH CH CH N i-Pr ClCF₃ Me CH CH CH N t-Bu Cl CF₃ Me CH CH CH N Et Cl CF₃ CF₃ CH CH CH Ni-Pr Cl CF₃ CF₃ CH CH CH N t-Bu Cl CF₃ CF₃ CH CH CH N Et Cl CF₃ OMe CHCH CH N i-Pr Cl CF₃ OMe CH CH CH N t-Bu Cl CF₃ OMe CH CH CH N Et Cl CF₃CN CH CH CH N i-Pr Cl CF₃ CN CH CH CH N t-Bu Cl CF₃ CN CH CH N CH Et MeCF₃ Cl CH CH N CH i-Pr Me CF₃ Cl CH CH N CH t-Bu Me CF₃ Cl CH CH N CH EtMe CF₃ Br CH CH N CH i-Pr Me CF₃ Br CH CH N CH t-Bu Me CF₃ Br CH CH N CHEt Me CF₃ I CH CH N CH i-Pr Me CF₃ I CH CH N CH t-Bu Me CF₃ I CH CH N CHEt Me CF₃ F CH CH N CH i-Pr Me CF₃ F CH CH N CH t-Bu Me CF₃ F CH CH N CHEt Me CF₃ Me CH CH N CH i-Pr Me CF₃ Me CH CH N CH t-Bu Me CF₃ Me CH CH NCH Et Me CF₃ CF₃ CH CH N CH i-Pr Me CF₃ CF₃ CH CH N CH t-Bu Me CF₃ CF₃CH CH N CH Et Me CF₃ OMe CH CH N CH i-Pr Me CF₃ OMe CH CH N CH t-Bu MeCF₃ OMe CH CH N CH Et Me CF₃ CN CH CH N CH i-Pr Me CF₃ CN CH CH N CHt-Bu Me CF₃ CN CH CH N CH Et Cl CF₃ Cl CH CH N CH i-Pr Cl CF₃ Cl CH CH NCH t-Bu Cl CF₃ Cl CH CH N CH Et Cl CF₃ Br CH CH N CH i-Pr Cl CF₃ Br CHCH N CH t-Bu Cl CF₃ Br CH CH N CH Et Cl CF₃ I CH CH N CH i-Pr Cl CF₃ ICH CH N CH t-Bu Cl CF₃ I CH CH N CH Et Cl CF₃ F CH CH N CH i-Pr Cl CF₃ FCH CH N CH t-Bu Cl CF₃ F CH CH N CH Et Cl CF₃ Me OH CH N CH i-Pr Cl CF₃Me CH CH N CH t-Bu Cl CF₃ Me CH CH N CH Et Cl CF₃ CF₃ CH CH N CH i-Pr ClCF₃ CF₃ CH CH N CH t-Bu Cl CF₃ CF₃ CH CH N CH Et Cl CF₃ OMe CH CH N CHi-Pr Cl CF₃ OMe CH CH N CH t-Bu Cl CF₃ OMe CH CH N CH Et Cl CF₃ CN CH CHN CH i-Pr Cl CF₃ CN CH CH N CH t-Bu Cl CF₃ CN CH N CH CH Et Me CF₃ Cl CHN CH CH i-Pr Me CF₃ Cl CH N CH CH t-Bu Me CF₃ Cl CH N CH CH Et Me CF₃ BrCH N CH CH i-Pr Me CF₃ Br CH N CH CH t-Bu Me CF₃ Br CH N CH CH Et Me CF₃I CH N CH CH i-Pr Me CF₃ I CH N CH CH t-Bu Me CF₃ I CH N CH CH Et Me CF₃F CH N CH CH i-Pr Me CF₃ F CH N CH CH t-Bu Me CF₃ F CH N CH CH Et Me CF₃Me CH N CH CH i-Pr Me CF₃ Me CH N CH CH t-Bu Me CF₃ Me CH N CH CH Et MeCF₃ CF₃ CH N CH CH i-Pr Me CF₃ CF₃ CH N CH CH t-Bu Me CF₃ CF₃ CH N CH CHEt Me CF₃ OMe CH N CH CH i-Pr Me CF₃ OMe CH N CH CH t-Bu Me CF₃ OMe CH NCH CH Et Me CF₃ CN CH N CH CH i-Pr Me CF₃ CN CH N CH CH t-Bu Me CF₃ CNCH N CH CH Et Cl CF₃ Cl CH N CH CH i-Pr Cl CF₃ Cl CH N CH CH t-Bu Cl CF₃Cl CH N CH CH Et Cl CF₃ Br CH N CH CH i-Pr Cl CF₃ Br CH N CH CH t-Bu ClCF₃ Br CH N CH CH Et Cl CF₃ I CH N CH CH i-Pr Cl CF₃ I CH N CH CH t-BuCl CF₃ I CH N CH CH Et Cl CF₃ F CH N CH CH i-Pr Cl CF₃ F CH N CH CH t-BuCl CF₃ F CH N CH CH Et Cl CF₃ Me CH N CH CH i-Pr Cl CF₃ Me CH N CH CHt-Bu Cl CF₃ Me CH N CH CH Et Cl CF₃ CF₃ CH N CH CH i-Pr Cl CF₃ CF₃ CH NCH CH t-Bu Cl CF₃ CF₃ CH N CH CH Et Cl CF₃ OMe CH N CH CH i-Pr Cl CF₃OMe CH N CH CH t-Bu Cl CF₃ OMe CH N CH CH Et Cl CF₃ CN CH N CH CH i-PrCl CF₃ CN CH N CH CH t-Bu Cl CF₃ CN N CH CH CH Et Me CF₃ Cl N CH CH CHi-Pr Me CF₃ Cl N CH CH CH t-Bu Me CF₃ Cl N CH CH CH Et Me CF₃ Br N CH CHCH i-Pr Me CF₃ Br N CH CH CH t-Bu Me CF₃ Br N CH CH CH Et Me CF₃ I N CHCH CH i-Pr Me CF₃ I N CH CH CH t-Bu Me CF₃ I N CH CH CH Et Me CF₃ F N CHCH C H i-Pr Me CF₃ F N CH CH CH t-Bu Me CF₃ F N CH CH CH Et Me CF₃ Me NCH CH CH i-Pr Me CF₃ Me N CH CH CH t-Bu Me CF₃ Me N CH CH CH Et Me CF₃CF₃ N CH CH CH i-Pr Me CF₃ CF₃ N CH CH CH t-Bu Me CF₃ CF₃ N CH CH CH EtMe CF₃ OMe N CH CH CH i-Pr Me CF₃ OMe N CH CH CH t-Bu Me CF₃ OMe N CH CHCH Et Me CF₃ CN N CH CH CH i-Pr Me CF₃ CN N CH CH CH t-Bu Me CF₃ CN N CHCH CH Et Cl CF₃ Cl N CH CH CH i-Pr Cl CF₃ Cl N CH CH CH t-Bu Cl CF₃ Cl NCH CH CH Et Cl CF₃ Br N CH CH CH i-Pr Cl CF₃ Br N CH CH CH t-Bu Cl CF₃Br N CH CH CH Et Cl CF₃ I N CH CH CH i-Pr Cl CF₃ I N CH CH CH t-Bu ClCF₃ I N CH CH CH Et Cl CF₃ F N CH CH CH i-Pr Cl CF₃ F N CH CH CH t-Bu ClCF₃ F N CH CH CH Et Cl CF₃ Me N CH CH CH i-Pr Cl CF₃ Me N CH CH CH t-BuCl CF₃ Me N CH CH CH Et Cl CF₃ CF₃ N CH CH CH i-Pr Cl CF₃ CF₃ N CH CH CHt-Bu Cl CF₃ CF₃ N CH CH CH Et Cl CF₃ OMe N CH CH CH i-Pr Cl CF₃ OMe N CHCH CH t-Bu Cl CF₃ OMe N CH CH CH Et Cl CF₃ CN N CH CH CH i-Pr Cl CF₃ CNN CH CH CH t-Bu Cl CF₃ CN CH N CH N Et Me CF₃ Cl CH N CH N i-Pr Me CF₃Cl CH N CH N t-Bu Me CF₃ Cl CH N CH N Et Me CF₃ Br CH N CH N i-Pr Me CF₃Br CH N CH N t-Bu Me CF₃ Br CH N CH N Et Me CF₃ I CH N CH N i-Pr Me CF₃I CH N CH N t-Bu Me CF₃ I CH N CH N Et Me CF₃ F CH N CH N i-Pr Me CF₃ FCH N CH N t-Bu Me CF₃ F CH N CH N Et Me CF₃ Me CH N CH N i-Pr Me CF₃ MeCH N CH N t-Bu Me CF₃ Me CH N CH N Et Me CF₃ CF₃ CH N CH N i-Pr Me CF₃CF₃ CH N CH N t-Bu Me CF₃ CF₃ CH N CH N Et Me CF₃ OMe CH N CH N i-Pr MeCF₃ OMe CH N CH N t-Bu Me CF₃ OMe CH N CH N Et Me CF₃ CN CH N CH N i-PrMe CF₃ CN CH N CH N t-Bu Me CF₃ CN CH N CH N Et Cl CF₃ Cl CH N CH N i-PrCl CF₃ Cl CH N CH N t-Bu Cl CF₃ Cl CH N CH N Et Cl CF₃ Br CH N CH N i-PrCl CF₃ Br CH N CH N t-Bu Cl CF₃ Br CH N CH N Et Cl CF₃ I CH N CH N i-PrCl CF₃ I CH N CH N t-Bu Cl CF₃ I CH N CH N Et Cl CF₃ F CH N CH N i-Pr ClCF₃ F CH N CH N t-Bu Cl CF₃ F CH N CH N Et Cl CF₃ Me CH N CH N i-Pr ClCF₃ Me CH N CH N t-Bu Cl CF₃ Me CH N CH N Et Cl CF₃ CF₃ CH N CH N i-PrCl CF₃ CF₃ CH N CH N t-Bu Cl CF₃ CF₃ CH N CH N Et Cl CF₃ OMe CH N CH Ni-Pr Cl CF₃ OMe CH N CH N t-Bu Cl CF₃ OMe CH N CH N Et Cl CF₃ CN CH N CHN i-Pr Cl CF₃ CN CH N CH N t-Bu Cl CF₃ CN CH CH CH CCl Et Me CF₃ Cl CHCH CH CCl i-Pr Me CF₃ Cl CH CH CH CCl t-Bu Me CF₃ Cl CH CH CH CCl Et MeCF₃ Br CH CH CH CCl i-Pr Me CF₃ Br CH CH CH CCl t-Bu Me CF₃ Br CH CH CHCCl Et Me CF₃ I CH CH CH CCl i-Pr Me CF₃ I CH CH CH CCl t-Bu Me CF₃ I CHCH CH CCl Et Me CF₃ F CH CH CH CCl i-Pr Me CF₃ F CH CH CR CCl t-Bu MeCF₃ F CH CH CH CCl Et Me CF₃ Me CH CH CH CCl i-Pr Me CF₃ Me CH CH CH CClt-Bu Me CF₃ Me CH CH CH CCl Et Me CF₃ CF₃ CH CH CH CCl i-Pr Me CF₃ CF₃CH CH CH CCl t-Bu Me CF₃ CF₃ CH CH CH CCl Et Me CF₃ OMe CH CH CH CCli-Pr Me CF₃ OMe CH CH CH CCl t-Bu Me CF₃ OMe CH CH CH CCl Et Me CF₃ CNCH CH CH CCl i-Pr Me CF₃ CN CH CH CH CCl t-Bu Me CF₃ CN CH CH CH CCl EtCl CF₃ Cl CH CH CH CCl i-Pr Cl CF₃ Cl CH CH CH CCl t-Bu Cl CF₃ Cl CH CHCH CCl Et Cl CF₃ Br CH CH CH CCl i-Pr Cl CF₃ Br CH CH CH CCl t-Bu Cl CF₃Br CH CH CH CCl Et Cl CF₃ I CH CH CH CCl i-Pr Cl CF₃ I CH CH CH CCl t-BuCl CF₃ I CH CH CH CCl Et Cl CF₃ F CH CH CH CCl i-Pr Cl CF₃ F CH CH CHCCl t-Bu Cl CF₃ F CH CH CH CCl Et Cl CF₃ Me CH CH CH CCl i-Pr Cl CF₃ MeCH CH CH CCl t-Bu Cl CF₃ Me CH CH CH CCl Et Cl CF₃ CF₃ CH CH CH CCl i-PrCl CF₃ CF₃ CH CH CH CCl t-Bu Cl CF₃ CF₃ CH CH CH CCl Et Cl CF₃ OMe CH CHCH CCl i-Pr Cl CF₃ OMe CH CH CH CCl t-Bu Cl CF₃ OMe CH CH CH CCl Et ClCF₃ CN CH CH CH CCl i-Pr Cl CF₃ CN CH CH CH CCl t-Bu Cl CF₃ CN CH CH CHCF Et Me CF₃ Cl CH CH CH CF i-Pr Me CF₃ Cl CH CH CH CF t-Bu Me CF₃ Cl CHCH CH CF Et Me CF₃ Br CH CH CH CF i-Pr Me CF₃ Br CH CH CH CF t-Bu Me CF₃Br CH CH CH CF Et Me CF₃ I CH CH CH CF i-Pr Me CF₃ I CH CH CH CF t-Bu MeCF₃ I CH CH CH CF Et Me CF₃ F CH CH CH CF i-Pr Me CF₃ F CH CH CH CF t-BuMe CF₃ F CH CH CH CF Et Me CF₃ Me CH CH CH CF i-Pr Me CF₃ Me CH CH CH CFt-Bu Me CF₃ Me CH CH CH CF Et Me CF₃ CF₃ CH CH CH CF i-Pr Me CF₃ CF₃ CHCH CH CF t-Bu Me CF₃ CF₃ CH CH CH CF Et Me CF₃ OMe CH CH CH CF i-Pr MeCF₃ OMe CH CH CH CF t-Bu Me CF₃ OMe CH CH CH CF Et Me CF₃ CN CH CH CH CFi-Pr Me CF₃ CN CH CH CH CF t-Bu Me CF₃ CN CH CH CH CF Et Cl CF₃ Cl CH CHCH CF i-Pr Cl CF₃ Cl CH CH CH CF t-Bu Cl CF₃ Cl CH CH CH CF Et Cl CF₃ BrCH CH CH CF i-Pr Cl CF₃ Br CH CH CH CF t-Bu Cl CF₃ Br CH CH CH CF Et ClCF₃ I CH CH CH CF i-Pr Cl CF₃ I CH CH CH CF t-Bu Cl CF₃ I CH CH CH CFi-Pr Cl CF₃ F CH CH CH CF t-Bu Cl CF₃ F CH CH CH CF Et Cl CF₃ Me CH CHCH CF i-Pr Cl CF₃ Me CH CH CH CF t-Bu Cl CF₃ Me CH CH CH CF Et Cl CF₃CF₃ CH CH CH CF i-Pr Cl CF₃ CF₃ CH CH CH CF t-Bu Cl CF₃ CF₃ CH CH CH CFEt Cl CF₃ OMe CH CH CH CF i-Pr Cl CF₃ OMe CH CH CH CF t-Bu Cl CF₃ OMe CHCH CH CF Et Cl CF₃ CN CH CH CH CF i-Pr Cl CF₃ CN CH CH CH CF t-Bu Cl CF₃CN CH CH CH CH Et Me C₂F₅ Cl CH CH CH CH i-Pr Me C₂F₅ Cl CH CH CH CHt-Bu Me C₂F₅ Cl CH CH CH CH Et Me C₂F₅ Br CH CH CH CH i-Pr Me C₂F₅ Br CHCH CH CH t-Bu Me C₂F₅ Br CH CH CH CH Et Me C₂F₅ I CH CH CH CH i-Pr MeC₂F₅ I CH CH CH CH t-Bu Me C₂F₅ I CH CH CH CH Et Me C₂F₅ F CH CH CH CHi-Pr Me C₂F₅ F CH CH CH CH t-Bu Me C₂F₅ F CH CH CH CH Et Me C₂F₅ Me CHCH CH CH i-Pr Me C₂F₅ Me CH CH CH CH t-Bu Me C₂F₅ Me CH CH CH CH Et MeC₂F₅ CF₃ CH CH CH CH i-Pr Me C₂F₅ CF₃ CH CH CH CH t-Bu Me C₂F₅ CF₃ CH CHCH CH Et Me C₂F₅ OMe CH CH CH CH i-Pr Me C₂F₅ OMe CH CH CH CH t-Bu MeC₂F₅ OMe CH CH CH CH Et Me C₂F₅ CN CH CH CH CH i-Pr Me C₂F₅ CN CH CH CHCH t-Bu Me C₂F₅ CN CH CH CH CH Et Cl C₂F₅ Cl CH CH CH CH i-Pr Cl C₂F₅ ClCH CH CH CH t-Bu Cl C₂F₅ Cl CH CH CH CH Et Cl C₂F₅ Br CH CH CH CH i-PrCl C₂F₅ Br CH CH CH CH t-Bu Cl C₂F₅ Br CH CH CH CH Et Cl C₂F₅ I CH CH CHCH i-Pr Cl C₂F₅ I CH CH CH CH t-Bu Cl C₂F₅ I CH CH CH CH Et Cl C₂F₅ F CHCH CH CH i-Pr Cl C₂F₅ F CH CH CH CH t-Bu Cl C₂F₅ F CH CH CH CH Et ClC₂F₅ Me CH CH CH CH i-Pr Cl C₂F₅ Me CH CH CH CH t-Bu Cl C₂F₅ Me CH CH CHCH Et Cl C₂F₅ CF₃ CH CH CH CH i-Pr Cl C₂F₅ CF₃ CH CH CH CH t-Bu Cl C₂F₅CF₃ CH CH CH CH Et Cl C₂F₅ OMe CH CH CH CH i-Pr Cl C₂F₅ OMe CH CH CH CHt-Bu Cl C₂F₅ OMe CH CH CH CH Et Cl C₂F₅ CN CH CH CH CH i-Pr Cl C₂F₅ CNCH CH CH CH t-Bu Cl C₂F₅ CN

[0351] TABLE 15

W X Y Z R³ R⁴ R⁷ R⁸ CH CH CH CH Et Me CF₃ Cl CH CH CH CH i-Pr Me CF₃ ClCH CH CH CH t-Bu Me CF₃ Cl CH CH CH CH Et Me CF₃ Br CH CH CH CH i-Pr MeCF₃ Br CH CH CH CH t-Bu Me CF₃ Br CH CH CH CH Et Me CF₃ I CH CH CH CHi-Pr Me CF₃ I CH CH CH CH t-Bu Me CF₃ I CH CH CH CH Et Me CF₃ F CH CH CHCH i-Pr Me CF₃ F CH CH CH CH t-Bu Me CF₃ F CH CH CH CH Et Me CF₃ Me CHCH CH CH i-Pr Me CF₃ Me CH CH CH CH t-Bu Me CF₃ Me CH CH CH CH Et Me CF₃CF₃ CH CH CH CH i-Pr Me CF₃ CF₃ CH CH CH CH t-Bu Me CF₃ CF₃ CH CH CH CHEt Me CF₃ OMe CH CH CH CH i-Pr Me CF₃ OMe CH CH CH CH t-Bu Me CF₃ OMe CHCH CH CH Et Me CF₃ CN CH CH CH CH i-Pr Me CF₃ CN CH CH CH CH t-Bu Me CF₃CN CH CH CH CH Et Cl CF₃ Cl CH CH CH CH i-Pr Cl CF₃ Cl CH CH CH CH t-BuCl CF₃ Cl CH CH CH CH Et Cl CF₃ Br CH CH CH CH i-Pr Cl CF₃ Br CH CH CHCH t-Bu Cl CF₃ Br CH CH CH CH Et Cl CF₃ I CH CH CH CH i-Pr Cl CF₃ I CHCH CH CH t-Bu Cl CF₃ I CH CH CH CH Et Cl CF₃ F CH CH CH CH i-Pr Cl CF₃ FCH CH CH CH t-Bu Cl CF₃ F CH CH CH CH Et Cl CF₃ Me CH CH CH CH i-Pr ClCF₃ Me CH CH CH CH t-Bu Cl CF₃ Me CH CH CH CH Et Cl CF₃ CF₃ CH CH CH CHi-Pr Cl CF₃ CF₃ CH CH CH CH t-Bu Cl CF₃ CF₃ CH CH CH CH Et Cl CF₃ OMe CHCH CH CH i-Pr Cl CF₃ OMe CH CH CH CH t-Bu Cl CF₃ OMe CH CH CH CH Et ClCF₃ CN CH CH CH CH i-Pr Cl CF₃ CN CH CH CH CH t-Bu Cl CF₃ CN CH CH CH NEt Me CF₃ Cl CH CH CH N i-Pr Me CF₃ Cl CH CH CH N t-Bu Me CF₃ Cl CH CHCH N Et Me CF₃ Br CH CH CH N i-Pr Me CF₃ Br CH CH CH N t-Bu Me CF₃ Br CHCH CH N Et Me CF₃ I CH CH CH N i-Pr Me CF₃ I CH CH CH N t-Bu Me CF₃ I CHCH CH N Et Me CF₃ F CH CH CH N i-Pr Me CF₃ F CH CH CH N t-Bu Me CF₃ F CHCH CH N Et Me CF₃ Me CH CH CH N i-Pr Me CF₃ Me CH CH CH N t-Bu Me CF₃ MeCH CH CH N Et Me CF₃ CF₃ CH CH CH N i-Pr Me CF₃ CF₃ CH CH CH N t-Bu MeCF₃ CF₃ CH CH CH N Et Me CF₃ OMe CH CH CH N i-Pr Me CF₃ OMe CH CH CH Nt-Bu Me CF₃ OMe CH CH CH N Et Me CF₃ CN CH CH CH N i-Pr Me CF₃ CN CH CHCH N t-Bu Me CF₃ CN CH CH CH N Et Cl CF₃ Cl CH CH CH N i-Pr Cl CF₃ Cl CHCH CH N t-Bu Cl CF₃ Cl CH CH CH N Et Cl CF₃ Br CH CH CH N i-Pr Cl CF₃ BrCH CH CH N t-Bu Cl CF₃ Br CH CH CH N Et Cl CF₃ I CH CH CH N i-Pr Cl CF₃I CH CH CH N t-Bu Cl CF₃ I CH CH CH N Et Cl CF₃ F CH CH CH N i-Pr Cl CF₃F CH CH CH N t-Bu Cl CF₃ F CH CH CH N Et Cl CF₃ Me CH CH CH N i-Pr ClCF₃ Me CH CH CH N t-Bu Cl CF₃ Me CH CH CH N Et Cl CF₃ CF₃ CH CH CH Ni-Pr Cl CF₃ CF₃ CH CH CH N t-Bu Cl CF₃ CF₃ CH CH CH N Et Cl CF₃ OMe CHCH CH N i-Pr Cl CF₃ OMe CH CH CH N t-Bu Cl CF₃ OMe CH CH CH N Et Cl CF₃CN CH CH CH N i-Pr Cl CF₃ CN CH CH CH N t-Bu Cl CF₃ CN CH CH N CH Et MeCF₃ Cl CH CH N CH i-Pr Me CF₃ Cl CH CH N CH t-Bu Me CF₃ Cl CH CH N CH EtMe CF₃ Br CH CH N CH i-Pr Me CF₃ Br CH CH N CH t-Bu Me CF₃ Br CH CH N CHEt Me CF₃ I CH CH N CH i-Pr Me CF₃ I CH CH N CH t-Bu Me CF₃ I CH CH N CHEt Me CF₃ F CH CH N CH i-Pr Me CF₃ F CH CH N CH t-Bu Me CF₃ F CH CH N CHEt Me CF₃ Me CH CH N CH i-Pr Me CF₃ Me CH CH N CH t-Bu Me CF₃ Me CH CH NCH Et Me CF₃ CF₃ CH CH N CH i-Pr Me CF₃ CF₃ CH CH N CH t-Bu Me CF₃ CF₃CH CH N CH Et Me CF₃ OMe CH CH N CH i-Pr Me CF₃ OMe CH CH N CH t-Bu MeCF₃ OMe CH CH N CH Et Me CF₃ CN CH CH N CH i-Pr Me CF₃ CN CH CH N CHt-Bu Me CF₃ CN CH CH N CH Et Cl CF₃ Cl CH CH N CH i-Pr Cl CF₃ Cl CH CH NCH t-Bu Cl CF₃ Cl CH CH N CH Et Cl CF₃ Br CH CH N CH i-Pr Cl CF₃ Br CHCH N CH t-Bu Cl CF₃ Br CH CH N CH Et Cl CF₃ I CH CH N CH i-Pr Cl CF₃ ICH CH N CH t-Bu Cl CF₃ I CH CH N CH Et Cl CF₃ F CH CH N CH i-Pr Cl CF₃ FCH CH N CH t-Bu Cl CF₃ F CH CH N CH Et Cl CF₃ Me CH CH N CH i-Pr Cl CF₃Me CH CH N CH t-Bu Cl CF₃ Me CH CH N CH Et Cl CF₃ CF₃ CH CH N CH i-Pr ClCF₃ CF₃ CH CH N CH t-Bu Cl CF₃ CF₃ CH CH N CH Et Cl CF₃ OMe CH CH N CHi-Pr Cl CF₃ OMe CH CH N CH t-Bu Cl CF₃ OMe CH CH N CH Et Cl CF₃ CN CH CHN CH i-Pr Cl CF₃ CN CH CH N CH t-Bu Cl CF₃ CN CH N CH CH Et Me CF₃ Cl CHN CH CH i-Pr Me CF₃ Cl CH N CH CH t-Bu Me CF₃ Cl CH N CH CH Et Me CF₃ BrCH N CH CH i-Pr Me CF₃ Br CH N CH CH t-Bu Me CF₃ Br CH N CH CH Et Me CF₃I CH N CH CH i-Pr Me CF₃ I CH N CH CH t-Bu Me CF₃ I CH N CH CH Et Me CF₃F CH N CH CH i-Pr Me CF₃ F CH N CH CH t-Bu Me CF₃ F CH N CH CH Et Me CF₃Me CH N CH CH i-Pr Me CF₃ Me CH N CH CH t-Bu Me CF₃ Me CH N CH CH Et MeCF₃ CF₃ CH N CH CH i-Pr Me CF₃ CF₃ CH N CH CH t-Bu Me CF₃ CF₃ CH N CH CHEt Me CF₃ OMe CH N CH CH i-Pr Me CF₃ OMe CH N CH CH t-Bu Me CF₃ OMe CH NCH CH Et Me CF₃ CN CH N CH CH i-Pr Me CF₃ CN CH N CH CH t-Bu Me CF₃ CNCH N CH CH Et Cl CF₃ Cl CH N CH CH i-Pr Cl CF₃ Cl CH N CH CH t-Bu Cl CF₃Cl CH N CH CH Et Cl CF₃ Br CH N CH CH i-Pr Cl CF₃ Br CH N CH CH t-Bu ClCF₃ Br CH N CH CH Et Cl CF₃ I CH N CH CH i-Pr Cl CF₃ I CH N CH CH t-BuCl CF₃ I CH N CH CH Et Cl CF₃ F CH N CH CH i-Pr Cl CF₃ F CH N CH CH t-BuCl CF₃ F CH N CH CH Et Cl CF₃ Me CH N CH CH i-Pr Cl CF₃ Me CH N CH CHt-Bu Cl CF₃ Me CH N CH CH Et Cl CF₃ CF₃ CH N CH CH i-Pr Cl CF₃ CF₃ CH NCH CH t-Bu Cl CF₃ CF₃ CH N CH CH Et Cl CF₃ OMe CH N CH CH i-Pr Cl CF₃OMe CH N CH CH t-Bu Cl CF₃ OMe CH N CH CH Et Cl CF₃ CN CH N CH CH i-PrCl CF₃ CN CH N CH CH t-Bu Cl CF₃ CN N CH CH CH Et Me CF₃ Cl N CH CH CHi-Pr Me CF₃ Cl N CH CH CH t-Bu Me CF₃ Cl N CH CH CH Et Me CF₃ Br N CH CHCH i-Pr Me CF₃ Br N CH CH CH t-Bu Me CF₃ Br N CH CH CH Et Me CF₃ I N CHCH CH i-Pr Me CF₃ I N CH CH CH t-Bu Me CF₃ I N CH CH CH Et Me CF₃ F N CHCH CH i-Pr Me CF₃ F N CH CH CH t-Bu Me CF₃ F N CH CH CH Et Me CF₃ Me NCH CH CH i-Pr Me CF₃ Me N CH CH CH t-Bu Me CF₃ Me N CH CH CH Et Me CF₃CF₃ N CH CH CH i-Pr Me CF₃ CF₃ N CH CH CH t-Bu Me CF₃ CF₃ N CH CH CH EtMe CF₃ OMe N CH CH CH i-Pr Me CF₃ OMe N CH CH CH t-Bu Me CF₃ OMe N CH CHCH Et Me CF₃ CN N CH CH CH i-Pr Me CF₃ CN N CH CH CH t-Bu Me CF₃ CN N CHCH CH Et Cl CF₃ Cl N CH CH CH i-Pr Cl CF₃ Cl N CH CH CH t-Bu Cl CF₃ Cl NCH CH CH Et Cl CF₃ Br N CH CH CH i-Pr Cl CF₃ Br N CH CH CH t-Bu Cl CF₃Br N CH CH CH Et Cl CF₃ I N CH CH CH i-Pr Cl CF₃ I N CH CH CH t-Bu ClCF₃ I N CH CH CH Et Cl CF₃ F N CH CH CH i-Pr Cl CF₃ F N CH CH CH t-Bu ClCF₃ F N CH CH CH Et Cl CF₃ Me N CH CH CH i-Pr Cl CF₃ Me N CH CH CH t-BuCl CF₃ Me N CH CH CH Et Cl CF₃ CF₃ N CH CH CH i-Pr Cl CF₃ CF₃ N CH CH CHt-Bu Cl CF₃ CF₃ N CH CH CH Et Cl CF₃ OMe N CH CH CH i-Pr Cl CF₃ OMe N CHCH CH t-Bu Cl CF₃ OMe N CH CH CH Et Cl CF₃ CN N CH CH CH i-Pr Cl CF₃ CNN CH CH CH t-Bu Cl CF₃ CN CH N CH N Et Me CF₃ Cl CH N CH N i-Pr Me CF₃Cl CH N CH N t-Bu Me CF₃ Cl CH N CH N Et Me CF₃ Br CH N CH N i-Pr Me CF₃Br CH N CH N t-Bu Me CF₃ Br CH N CH N Et Me CF₃ I CH N CH N i-Pr Me CF₃I CH N CH N t-Bu Me CF₃ I CH N CH N Et Me CF₃ F CH N CH N i-Pr Me CF₃ FCH N CH N t-Bu Me CF₃ F CH N CH N Et Me CF₃ Me CH N CH N i-Pr Me CF₃ MeCH N CH N t-Bu Me CF₃ Me CH N CH N Et Me CF₃ CF₃ CH N CH N i-Pr Me CF₃CF₃ CH N CH N t-Bu Me CF₃ CF₃ CH N CH N Et Me CF₃ OMe CH N CH N i-Pr MeCF₃ OMe CH N CH N t-Bu Me CF₃ OMe CH N CH N Et Me CF₃ CN CH N CH N i-PrMe CF₃ CN CH N CH N t-Bu Me CF₃ CN CH N CH N Et Cl CF₃ Cl CH N CH N i-PrCl CF₃ Cl CH N CH N t-Bu Cl CF₃ Cl CH N CH N Et Cl CF₃ Br CH N CH N i-PrCl CF₃ Br CH N CH N t-Bu Cl CF₃ Br CH N CH N Et Cl CF₃ I CH N CH N i-PrCl CF₃ I CH N CH N t-Bu Cl CF₃ I CH N CH N Et Cl CF₃ F CH N CH N i-Pr ClCF₃ F CH N CH N t-Bu Cl CF₃ F CH N CH N Et Cl CF₃ Me CH N CH N i-Pr ClCF₃ Me CH N CH N t-Bu Cl CF₃ Me CH N CH N Et Cl CF₃ CF₃ CH N CH N i-PrCl CF₃ CF₃ CH N CH N t-Bu Cl CF₃ CF₃ CH N CH N Et Cl CF₃ OMe CH N CH Ni-Pr Cl CF₃ OMe CH N CH N t-Bu Cl CF₃ OMe CH N CH N Et Cl CF₃ CN CH N CHN i-Pr Cl CF₃ CN CH N CH N t-Bu Cl CF₃ CN CH CH CH CCl Et Me CF₃ Cl CHCH CH CCl i-Pr Me CF₃ Cl CH CH CH CCl t-Bu Me CF₃ Cl CH CH CH CCl Et MeCF₃ Br CH CH CH CCl i-Pr Me CF₃ Br CH CH CH CCl t-Bu Me CF₃ Br CH CH CHCCl Et Me CF₃ I CH CH CH CCl i-Pr Me CF₃ I CH CH CH CCl t-Bu Me CF₃ I CHCH CH CCl Et Me CF₃ F CH CH CH CCl i-Pr Me CF₃ F CH CH CH CCl t-Bu MeCF₃ F CH CH CH CCl Et Me CF₃ Me CH CH CH CCl i-Pr Me CF₃ Me CH CH CH CClt-Bu Me CF₃ Me CH CH CH CCl Et Me CF₃ CF₃ CH CH CH CCl i-Pr Me CF₃ CF₃CH CH CH CCl t-Bu Me CF₃ CF₃ CH CH CH CCl Et Me CF₃ OMe CH CH CH CCli-Pr Me CF₃ OMe CH CH CH CCl t-Bu Me CF₃ OMe CH CH CH CCl Et Me CF₃ CNCH CH CH CCl i-Pr Me CF₃ CN CH CH CH CCl t-Bu Me CF₃ CN CH CH CH CCl EtCl CF₃ Cl CH CH CH CCl i-Pr Cl CF₃ Cl CH CH CH CCl t-Bu Cl CF₃ Cl CH CHCH CCl Et Cl CF₃ Br CH CH CH CCl i-Pr Cl CF₃ Br CH CH CH CCl t-Bu Cl CF₃Br CH CH CH CCl Et Cl CF₃ I CH CH CH CCl i-Pr Cl CF₃ I CH CH CH CCl t-BuCl CF₃ I CH CH CH CCl Et Cl CF₃ F CH CH CH CCl i-Pr Cl CF₃ F CH CH CHCCl t-Bu Cl CF₃ F CH CH CH CCl Et Cl CF₃ Me CH CH CH CCl i-Pr Cl CF₃ MeCH CH CH CCl t-Bu Cl CF₃ Me CH CH CH CCl Et Cl CF₃ CF₃ CH CH CH CCl i-PrCl CF₃ CF₃ CH CH CH CCl t-Bu Cl CF₃ CF₃ CH CH CH CCl Et Cl CF₃ OMe CH CHCH CCl i-Pr Cl CF₃ OMe CH CH CH CCl t-Bu Cl CF₃ OMe CH CH CH CCl Et ClCF₃ CN CH CH CH CCl i-Pr Cl CF₃ CN CH CH CH CCl t-Bu Cl CF₃ CN CH CH CHCF Et Me CF₃ Cl CH CH CH CF i-Pr Me CF₃ Cl CH CH CH CF t-Bu Me CF₃ Cl CHCH CH CF Et Me CF₃ Br CH CH CH CF i-Pr Me CF₃ Br CH CH CH CF t-Bu Me CF₃Br CH CH CH CF Et Me CF₃ I CH CH CH CF i-Pr Me CF₃ I CH CH CH CF t-Bu MeCF₃ I CH CH CH CF Et Me CF₃ F CH CH CH CF i-Pr Me CF₃ F CH CH CH CF t-BuMe CF₃ F CH CH CH CF Et Me CF₃ Me CH CH CH CF i-Pr Me CF₃ Me CH CH CH CFt-Bu Me CF₃ Me CH CH CH CF Et Me CF₃ CF₃ CH CH CH CF i-Pr Me CF₃ CF₃ CHCH CH CF t-Bu Me CF₃ CF₃ CH CH CH CF Et Me CF₃ OMe CH CH CH CF i-Pr MeCF₃ OMe CH CH CH CF t-Bu Me CF₃ OMe CH CH CH CF Et Me CF₃ CN CH CH CH CFi-Pr Me CF₃ CN CH CH CH CF t-Bu Me CF₃ CN CH CH CH CF Et Cl CF₃ Cl CH CHCH CF i-Pr Cl CF₃ Cl CH CH CH CF t-Bu Cl CF₃ Cl CH CH CH CF Et Cl CF₃ BrCH CH CH CF i-Pr Cl CF₃ Br CH CH CH CF t-Bu Cl CF₃ Br CH CH CH CF Et ClCF₃ I CH CH CH CF i-Pr Cl CF₃ I CH CH CH CF t-Bu Cl CF₃ I CH CH CH CFi-Pr Cl CF₃ F CH CH CH CF t-Bu Cl CF₃ F CH CH CH CF Et Cl CF₃ Me CH CHCH CF i-Pr Cl CF₃ Me CH CH CH CF t-Bu Cl CF₃ Me CH CH CH CF Et Cl CF₃CF₃ CH CH CH CF i-Pr Cl CF₃ CF₃ CH CH CH CF t-Bu Cl CF₃ CF₃ CH CH CH CFEt Cl CF₃ OMe CH CH CH CF i-Pr Cl CF₃ OMe CH CH CH CF t-Bu Cl CF₃ OMe CHCH CH CF Et Cl CF₃ CN CH CH CH CF i-Pr Cl CF₃ CN CH CH CH CF t-Bu Cl CF₃CN CH CH CH CH Et Me C₂F₅ Cl CH CH CH CH i-Pr Me C₂F₅ Cl CH CH CH CHt-Bu Me C₂F₅ Cl CH CH CH CH Et Me C₂F₅ Br CH CH CH CH i-Pr Me C₂F₅ Br CHCH CH CH t-Bu Me C₂F₅ Br CH CH CH CH Et Me C₂F₅ I CH CH CH CH i-Pr MeC₂F₅ I CH CH CH CH t-Bu Me C₂F₅ I CH CH CH CH Et Me C₂F₅ F CH CH CH CHi-Pr Me C₂F₅ F CH CH CH CH t-Bu Me C₂F₅ F CH CH CH CH Et Me C₂F₅ Me CHCH CH CH i-Pr Me C₂F₅ Me CH CH CH CH t-Bu Me C₂F₅ Me CH CH CH CH Et MeC₂F₅ CF₃ CH CH CH CH i-Pr Me C₂F₅ CF₃ CH CH CH CH t-Bu Me C₂F₅ CF₃ CH CHCH CH Et Me C₂F₅ OMe CH CH CH CH i-Pr Me C₂F₅ OMe CH CH CH CH t-Bu MeC₂F₅ OMe CH CH CH CH Et Me C₂F₅ CN CH CH CH CH i-Pr Me C₂F₅ CN CH CH CHCH t-Bu Me C₂F₅ CN CH CH CH CH Et Cl C₂F₅ Cl CH CH CH CH i-Pr Cl C₂F₅ ClCH CH CH CH t-Bu Cl C₂F₅ Cl CH CH CH CH Et Cl C₂F₅ Br CH CH CH CH i-PrCl C₂F₅ Br CH CH CH CH t-Bu Cl C₂F₅ Br CH CH CH CH Et Cl C₂F₅ I CH CH CHCH i-Pr Cl C₂F₅ I CH CH CH CH t-Bu Cl C₂F₅ I CH CH CH CH Et Cl C₂F₅ F CHCH CH CH i-Pr Cl C₂F₅ F CH CH CH CH t-Bu Cl C₂F₅ F CH CH CH CH Et ClC₂F₅ Me CH CH CH CH i-Pr Cl C₂F₅ Me CH CH CH CH t-Bu Cl C₂F₅ Me CH CH CHCH Et Cl C₂F₅ CF₃ CH CH CH CH i-Pr Cl C₂F₅ CF₃ CH CH CH CH t-Bu Cl C₂F₅CF₃ CH CH CH CH Et Cl C₂F₅ OMe CH CH CH CH i-Pr Cl C₂F₅ OMe CH CH CH CHt-Bu Cl C₂F₅ OMe CH CH CH CH Et Cl C₂F₅ CN CH CH CH CH i-Pr Cl C₂F₅ CNCH CH CH CH t-Bu Cl C₂F₅ CN

[0352] TABLE 16

W X Y Z R³ R⁴ R⁷ R⁸ CH CH CH CH Et Me CF₃ Cl CH CH CH CH i-Pr Me CF₃ ClCH CH CH CH t-Bu Me CF₃ Cl CH CH CH CH Et Me CF₃ Br CH CH CH CH i-Pr MeCF₃ Br CH CH CH CH t-Bu Me CF₃ Br CH CH CH CH Et Me CF₃ I CH CH CH CHi-Pr Me CF₃ I CH CH CH CH t-Bu Me CF₃ I CH CH CH CH Et Me CF₃ F CH CH CHCH i-Pr Me CF₃ F CH CH CH CH t-Bu Me CF₃ F CH CH CH CH Et Me CF₃ Me CHCH CH CH i-Pr Me CF₃ Me CH CH CH CH t-Bu Me CF₃ Me CH CH CH CH Et Me CF₃CF₃ CH CH CH CH i-Pr Me CF₃ CF₃ CH CH CH CH t-Bu Me CF₃ CF₃ CH CH CH CHEt Me CF₃ OMe CH CH CH CH i-Pr Me CF₃ OMe CH CH CH CH t-Bu Me CF₃ OMe CHCH CH CH Et Me CF₃ CN CH CH CH CH i-Pr Me CF₃ CN CH CH CH CH t-Bu Me CF₃CN CH CH CH CH Et Cl CF₃ Cl CH CH CH CH i-Pr Cl CF₃ Cl CH CH CH CH t-BuCl CF₃ Cl CH CH CH CH Et Cl CF₃ Br CH CH CH CH i-Pr Cl CF₃ Br CH CH CHCH t-Bu Cl CF₃ Br CH CH CH CH Et Cl CF₃ I CH CH CH CH i-Pr Cl CF₃ I CHCH CH CH t-Bu Cl CF₃ I CH CH CH CH Et Cl CF₃ F CH CH CH CH i-Pr Cl CF₃ FCH CH CH CH t-Bu Cl CF₃ F CH CH CH CH Et Cl CF₃ Me CH CH CH CH i-Pr ClCF₃ Me CH CH CH CH t-Bu Cl CF₃ Me CH CH CH CH Et Cl CF₃ CF₃ CH CH CH CHi-Pr Cl CF₃ CF₃ CH CH CH CH t-Bu Cl CF₃ CF₃ CH CH CH CH Et Cl CF₃ OMe CHCH CH CH i-Pr Cl CF₃ OMe CH CH CH CH t-Bu Cl CF₃ OMe CH CH CH CH Et ClCF₃ CN CH CH CH CH i-Pr Cl CF₃ CN CH CH CH CH t-Bu Cl CF₃ CN CH CH CH NEt Me CF₃ Cl CH CH CH N i-Pr Me CF₃ Cl CH CH CH N t-Bu Me CF₃ Cl CH CHCH N Et Me CF₃ Br CH CH CH N i-Pr Me CF₃ Br CH CH CH N t-Bu Me CF₃ Br CHCH CH N Et Me CF₃ I CH CH CH N i-Pr Me CF₃ I CH CH CH N t-Bu Me CF₃ I CHCH CH N Et Me CF₃ F CH CH CH N i-Pr Me CF₃ F CH CH CH N t-Bu Me CF₃ F CHCH CH N Et Me CF₃ Me CH CH CH N i-Pr Me CF₃ Me CH CH CH N t-Bu Me CF₃ MeCH CH CH N Et Me CF₃ CF₃ CH CH CH N i-Pr Me CF₃ CF₃ CH CH CH N t-Bu MeCF₃ CF₃ CH CH CH N Et Me CF₃ OMe CH CH CH N i-Pr Me CF₃ OMe CH CH CH Nt-Bu Me CF₃ OMe CH CH CH N Et Me CF₃ CN CH CH CH N i-Pr Me CF₃ CN CH CHCH N t-Bu Me CF₃ CN CH CH CH N Et Cl CF₃ Cl CH CH CH N i-Pr Cl CF₃ Cl CHCH CH N t-Bu Cl CF₃ Cl CH CH CH N Et Cl CF₃ Br CH CH CH N i-Pr Cl CF₃ BrCH CH CH N t-Bu Cl CF₃ Br CH CH CH N Et Cl CF₃ I CH CH CH N i-Pr Cl CF₃I CH CH CH N t-Bu Cl CF₃ I CH CH CH N Et Cl CF₃ F CH CH CH N i-Pr Cl CF₃F CH CH CH N t-Bu Cl CF₃ F CH CH CH N Et Cl CF₃ Me CH CH CH N i-Pr ClCF₃ Me CH CH CH N t-Bu Cl CF₃ Me CH CH CH N Et Cl CF₃ CF₃ CH CH CH Ni-Pr Cl CF₃ CF₃ CH CH CH N t-Bu Cl CF₃ CF₃ CH CH CH N Et Cl CF₃ OMe CHCH CH N i-Pr Cl CF₃ OMe CH CH CH N t-Bu Cl CF₃ OMe CH CH CH N Et Cl CF₃CN CH CH CH N i-Pr Cl CF₃ CN CH CH CH N t-Bu Cl CF₃ CN CH CH N CH Et MeCF₃ Cl CH CH N CH i-Pr Me CF₃ Cl CH CH N CH t-Bu Me CF₃ Cl CH CH N CH EtMe CF₃ Br CH CH N CH i-Pr Me CF₃ Br CH CH N CH t-Bu Me CF₃ Br CH CH N CHEt Me CF₃ I CH CH N CH i-Pr Me CF₃ I CH CH N CH t-Bu Me CF₃ I CH CH N CHEt Me CF₃ F CH CH N CH i-Pr Me CF₃ F CH CH N CH t-Bu Me CF₃ F CH CH N CHEt Me CF₃ Me CH CH N CH i-Pr Me CF₃ Me CH CH N CH t-Bu Me CF₃ Me CH CH NCH Et Me CF₃ CF₃ CH CH N CH i-Pr Me CF₃ CF₃ CH CH N CH t-Bu Me CF₃ CF₃CH CH N CH Et Me CF₃ OMe CH CH N CH i-Pr Me CF₃ OMe CH CH N CH t-Bu MeCF₃ OMe CH CH N CH Et Me CF₃ CN CH CH N CH i-Pr Me CF₃ CN CH CH N CHt-Bu Me CF₃ CN CH CH N CH Et Cl CF₃ Cl CH CH N CH i-Pr Cl CF₃ Cl CH CH NCH t-Bu Cl CF₃ Cl CH CH N CH Et Cl CF₃ Br CH CH N CH i-Pr Cl CF₃ Br CHCH N CH t-Bu Cl CF₃ Br CH CH N CH Et Cl CF₃ I CH CH N CH i-Pr Cl CF₃ ICH CH N CH t-Bu Cl CF₃ I CH CH N CH Et Cl CF₃ F CH CH N CH i-Pr Cl CF₃ FCH CH N CH t-Bu Cl CF₃ F CH CH N CH Et Cl CF₃ Me CH CH N CH i-Pr Cl CF₃Me CH CH N CH t-Bu Cl CF₃ Me CH CH N CH Et Cl CF₃ CF₃ CH CH N CH i-Pr ClCF₃ CF₃ CH CH N CH t-Bu Cl CF₃ CF₃ CH CH N CH Et Cl CF₃ OMe CH CH N CHi-Pr Cl CF₃ OMe CH CH N CH t-Bu Cl CF₃ OMe CH CH N CH Et Cl CF₃ CN CH CHN CH i-Pr Cl CF₃ CN CH CH N CH t-Bu Cl CF₃ CN CH N CH CH Et Me CF₃ Cl CHN CH CH i-Pr Me CF₃ Cl CH N CH CH t-Bu Me CF₃ Cl CH N CH CH Et Me CF₃ BrCH N CH CH i-Pr Me CF₃ Br CH N CH CH t-Bu Me CF₃ Br CH N CH CH Et Me CF₃I CH N CH CH i-Pr Me CF₃ I CH N CH CH t-Bu Me CF₃ I CH N CH CH Et Me CF₃F CH N CH CH i-Pr Me CF₃ F CH N CH CH t-Bu Me CF₃ F CH N CH CH Et Me CF₃Me CH N CH CH i-Pr Me CF₃ Me CH N CH CH t-Bu Me CF₃ Me CH N CH CH Et MeCF₃ CF₃ CH N CH CH i-Pr Me CF₃ CF₃ CH N CH CH t-Bu Me CF₃ CF₃ CH N CH CHEt Me CF₃ OMe CH N CH CH i-Pr Me CF₃ OMe CH N CH CH t-Bu Me CF₃ OMe CH NCH CH Et Me CF₃ CN CH N CH CH i-Pr Me CF₃ CN CH N CH CH t-Bu Me CF₃ CNCH N CH CH Et Cl CF₃ Cl CH N CH CH i-Pr Cl CF₃ Cl CH N CH CH t-Bu Cl CF₃Cl CH N CH CH Et Cl CF₃ Br CH N CH CH i-Pr Cl CF₃ Br CH N CH CH t-Bu ClCF₃ Br CH N CH CH Et Cl CF₃ I CH N CH CH i-Pr Cl CF₃ I CH N CH CH t-BuCl CF₃ I CH N CH CH Et Cl CF₃ F CH N CH CH i-Pr Cl CF₃ F CH N CH CH t-BuCl CF₃ F CH N CH CH Et Cl CF₃ Me CH N CH CH i-Pr Cl CF₃ Me CH N CH CHt-Bu Cl CF₃ Me CH N CH CH Et Cl CF₃ CF₃ CH N CH CH i-Pr Cl CF₃ CF₃ CH NCH CH t-Bu Cl CF₃ CF₃ CH N CH CH Et Cl CF₃ OMe CH N CH CH i-Pr Cl CF₃OMe CH N CH CH t-Bu Cl CF₃ OMe CH N CH CH Et Cl CF₃ CN CH N CH CH i-PrCl CF₃ CN CH N CH CH t-Bu Cl CF₃ CN N CH CH CH Et Me CF₃ Cl N CH CH CHi-Pr Me CF₃ Cl N CH CH CH t-Bu Me CF₃ Cl N CH CH CH Et Me CF₃ Br N CH CHCH i-Pr Me CF₃ Br N CH CH CH t-Bu Me CF₃ Br N CH CH CH Et Me CF₃ I N CHCH CH i-Pr Me CF₃ I N CH CH CH t-Bu Me CF₃ I N CH CH CH Et Me CF₃ F N CHCH CH i-Pr Me CF₃ F N CH CH CH t-Bu Me CF₃ F N CH CH CH Et Me CF₃ Me NCH CH CH i-Pr Me CF₃ Me N CH CH CH t-Bu Me CF₃ Me N CH CH CH Et Me CF₃CF₃ N CH CH CH i-Pr Me CF₃ CF₃ N CH CH CH t-Bu Me CF₃ CF₃ N CH CH CH EtMe CF₃ OMe N CH CH CH i-Pr Me CF₃ OMe N CH CH CH t-Bu Me CF₃ OMe N CH CHCH Et Me CF₃ CN N CH CH CH i-Pr Me CF₃ CN N CH CH CH t-Bu Me CF₃ CN N CHCH CH Et Cl CF₃ Cl N CH CH CH i-Pr Cl CF₃ Cl N CH CH CH t-Bu Cl CF₃ Cl NCH CH CH Et Cl CF₃ Br N CH CH CH i-Pr Cl CF₃ Br N CH CH CH t-Bu Cl CF₃Br N CH CH CH Et Cl CF₃ I N CH CH CH i-Pr Cl CF₃ I N CH CH CH t-Bu ClCF₃ I N CH CH CH Et Cl CF₃ F N CH CH CH i-Pr Cl CF₃ F N CH CH CH t-Bu ClCF₃ F N CH CH CH Et Cl CF₃ Me N CH CH CH i-Pr Cl CF₃ Me N CH CH CH t-BuCl CF₃ Me N CH CH CH Et Cl CF₃ CF₃ N CH CH CH i-Pr Cl CF₃ CF₃ N CH CH CHt-Bu Cl CF₃ CF₃ N CH CH CH Et Cl CF₃ OMe N CH CH CH i-Pr Cl CF₃ OMe N CHCH CH t-Bu Cl CF₃ OMe N CH CH CH Et Cl CF₃ CN N CH CH CH i-Pr Cl CF₃ CNN CH CH CH t-Bu Cl CF₃ CN CH N CH N Et Me CF₃ Cl CH N CH N i-Pr Me CF₃Cl CH N CH N t-Bu Me CF₃ Cl CH N CH N Et Me CF₃ Br CH N CH N i-Pr Me CF₃Br CH N CH N t-Bu Me CF₃ Br CH N CH N Et Me CF₃ I CH N CH N i-Pr Me CF₃I CH N CH N t-Bu Me CF₃ I CH N CH N Et Me CF₃ F CH N CH N i-Pr Me CF₃ FCH N CH N t-Bu Me CF₃ F CH N CH N Et Me CF₃ Me CH N CH N i-Pr Me CF₃ MeCH N CH N t-Bu Me CF₃ Me CH N CH N Et Me CF₃ CF₃ CH N CH N i-Pr Me CF₃CF₃ CH N CH N t-Bu Me CF₃ CF₃ CH N CH N Et Me CF₃ OMe CH N CH N i-Pr MeCF₃ OMe CH N CH N t-Bu Me CF₃ OMe CH N CH N Et Me CF₃ CN CH N CH N i-PrMe CF₃ CN CH N CH N t-Bu Me CF₃ CN CH N CH N Et Cl CF₃ Cl CH N CH N i-PrCl CF₃ Cl CH N CH N t-Bu Cl CF₃ Cl CH N CH N Et Cl CF₃ Br CH N CH N i-PrCl CF₃ Br CH N CH N t-Bu Cl CF₃ Br CH N CH N Et Cl CF₃ I CH N CH N i-PrCl CF₃ I CH N CH N t-Bu Cl CF₃ I CH N CH N Et Cl CF₃ F CH N CH N i-Pr ClCF₃ F CH N CH N t-Bu Cl CF₃ F CH N CH N Et Cl CF₃ Me CH N CH N i-Pr ClCF₃ Me CH N CH N t-Bu Cl CF₃ Me CH N CH N Et Cl CF₃ CF₃ CH N CH N i-PrCl CF₃ CF₃ CH N CH N t-Bu Cl CF₃ CF₃ CH N CH N Et Cl CF₃ OMe CH N CH Ni-Pr Cl CF₃ OMe CH N CH N t-Bu Cl CF₃ OMe CH N CH N Et Cl CF₃ CN CH N CHN i-Pr Cl CF₃ CN CH N CH N t-Bu Cl CF₃ CN CH CH CH CCl Et Me CF₃ Cl CHCH CH CCl i-Pr Me CF₃ Cl CH CH CH CCl t-Bu Me CF₃ Cl CH CH CH CCl Et MeCF₃ Br CH CH CH CCl i-Pr Me CF₃ Br CH CH CH CCl t-Bu Me CF₃ Br CH CH CHCCl Et Me CF₃ I CH CH CH CCl i-Pr Me CF₃ I CH CH CH CCl t-Bu Me CF₃ I CHCH CH CCl Et Me CF₃ F CH CH CH CCl i-Pr Me CF₃ F CH CH CH CCl t-Bu MeCF₃ F CH CH CH CCl Et Me CF₃ Me CH CH CH CCl i-Pr Me CF₃ Me CH CH CH CClt-Bu Me CF₃ Me CH CH CH CCl Et Me CF₃ CF₃ CH CH CH CCl i-Pr Me CF₃ CF₃CH CH CH CCl t-Bu Me CF₃ CF₃ CH CH CH CCl Et Me CF₃ OMe CH CH CH CCli-Pr Me CF₃ OMe CH CH CH CCl t-Bu Me CF₃ OMe CH CH CH CCl Et Me CF₃ CNCH CH CH CCl i-Pr Me CF₃ CN CH CH CH CCl t-Bu Me CF₃ CN CH CH CH CCl EtCl CF₃ Cl CH CH CH CCl i-Pr Cl CF₃ Cl CH CH CH CCl t-Bu Cl CF₃ Cl CH CHCH CCl Et Cl CF₃ Br CH CH CH CCl i-Pr Cl CF₃ Br CH CH CH CCl t-Bu Cl CF₃Br CH CH CH CCl Et Cl CF₃ I CH CH CH CCl i-Pr Cl CF₃ I CH CH CH CCl t-BuCl CF₃ I CH CH CH CCl Et Cl CF₃ F CH CH CH CCl i-Pr Cl CF₃ F CH CH CHCCl t-Bu Cl CF₃ F CH CH CH CCl Et Cl CF₃ Me CH CH CH CCl i-Pr Cl CF₃ MeCH CH CH CCl t-Bu Cl CF₃ Me CH CH CH CCl Et Cl CF₃ CF₃ CH CH CH CCl i-PrCl CF₃ CF₃ CH CH CH CCl t-Bu Cl CF₃ CF₃ CH CH CH CCl Et Cl CF₃ OMe CH CHCH CCl i-Pr Cl CF₃ OMe CH CH CH CCl t-Bu Cl CF₃ OMe CH CH CH CCl Et ClCF₃ CN CH CH CH CCl i-Pr Cl CF₃ CN CH CH CH CCl t-Bu Cl CF₃ CN CH CH CHCF Et Me CF₃ Cl CH CH CH CF i-Pr Me CF₃ Cl CH CH CH CF t-Bu Me CF₃ Cl CHCH CH CF Et Me CF₃ Br CH CH CH CF i-Pr Me CF₃ Br CH CH CH CF t-Bu Me CF₃Br CH CH CH CF Et Me CF₃ I CH CH CH CF i-Pr Me CF₃ I CH CH CH CF t-Bu MeCF₃ I CH CH CH CF Et Me CF₃ F CH CH CH CF i-Pr Me CF₃ F CH CH CH CF t-BuMe CF₃ F CH CH CH CF Et Me CF₃ Me CH CH CH CF i-Pr Me CF₃ Me CH CH CH CFt-Bu Me CF₃ Me CH CH CH CF Et Me CF₃ CF₃ CH CH CH CF i-Pr Me CF₃ CF₃ CHCH CH CF t-Bu Me CF₃ CF₃ CH CH CH CF Et Me CF₃ OMe CH CH CH CF i-Pr MeCF₃ OMe CH CH CH CF t-Bu Me CF₃ OMe CH CH CH CF Et Me CF₃ CN CH CH CH CFi-Pr Me CF₃ CN CH CH CH CF t-Bu Me CF₃ CN CH CH CH CF Et Cl CF₃ Cl CH CHCH CF i-Pr Cl CF₃ Cl CH CH CH CF t-Bu Cl CF₃ Cl CH CH CH CF Et Cl CF₃ BrCH CH CH CF i-Pr Cl CF₃ Br CH CH CH CF t-Bu Cl CF₃ Br CH CH CH CF Et ClCF₃ I CH CH CH CF i-Pr Cl CF₃ I CH CH CH CF t-Bu Cl CF₃ I CH CH CH CFi-Pr Cl CF₃ F CH CH CH CF t-Bu Cl CF₃ F CH CH CH CF Et Cl CF₃ Me CH CHCH CF i-Pr Cl CF₃ Me CH CH CH CF t-Bu Cl CF₃ Me CH CH CH CF Et Cl CF₃CF₃ CH CH CH CF i-Pr Cl CF₃ CF₃ CH CH CH CF t-Bu Cl CF₃ CF₃ CH CH CH CFEt Cl CF₃ OMe CH CH CH CF i-Pr Cl CF₃ OMe CH CH CH CF t-Bu Cl CF₃ OMe CHCH CH CF Et Cl CF₃ CN CH CH CH CF i-Pr Cl CF₃ CN CH CH CH CF t-Bu Cl CF₃CN CH CH CH CH Et Me C₂F₅ Cl CH CH CH CH i-Pr Me C₂F₅ Cl CH CH CH CHt-Bu Me C₂F₅ Cl CH CH CH CH Et Me C₂F₅ Br CH CH CH CH i-Pr Me C₂F₅ Br CHCH CH CH t-Bu Me C₂F₅ Br CH CH CH CH Et Me C₂F₅ I CH CH CH CH i-Pr MeC₂F₅ I CH CH CH CH t-Bu Me C₂F₅ I CH CH CH CH Et Me C₂F₅ F CH CH CH CHi-Pr Me C₂F₅ F CH CH CH CH t-Bu Me C₂F₅ F CH CH CH CH Et Me C₂F₅ Me CHCH CH CH i-Pr Me C₂F₅ Me CH CH CH CH t-Bu Me C₂F₅ Me CH CH CH CH Et MeC₂F₅ CF₃ CH CH CH CH i-Pr Me C₂F₅ CF₃ CH CH CH CH t-Bu Me C₂F₅ CF₃ CH CHCH CH Et Me C₂F₅ OMe CH CH CH CH i-Pr Me C₂F₅ OMe CH CH CH CH t-Bu MeC₂F₅ OMe CH CH CH CH Et Me C₂F₅ CN CH CH CH CH i-Pr Me C₂F₅ CN CH CH CHCH t-Bu Me C₂F₅ CN CH CH CH CH Et Cl C₂F₅ Cl CH CH CH CH i-Pr Cl C₂F₅ ClCH CH CH CH t-Bu Cl C₂F₅ Cl CH CH CH CH Et Cl C₂F₅ Br CH CH CH CH i-PrCl C₂F₅ Br CH CH CH CH t-Bu Cl C₂F₅ Br CH CH CH CH Et Cl C₂F₅ I CH CH CHCH i-Pr Cl C₂F₅ I CH CH CH CH t-Bu Cl C₂F₅ I CH CH CH CH Et Cl C₂F₅ F CHCH CH CH i-Pr Cl C₂F₅ F CH CH CH CH t-Bu Cl C₂F₅ F CH CH CH CH Et ClC₂F₅ Me CH CH CH CH i-Pr Cl C₂F₅ Me CH CH CH CH t-Bu Cl C₂F₅ Me CH CH CHCH Et Cl C₂F₅ CF₃ CH CH CH CH i-Pr Cl C₂F₅ CF₃ CH CH CH CH t-Bu Cl C₂F₅CF₃ CH CH CH CH Et Cl C₂F₅ OMe CH CH CH CH i-Pr Cl C₂F₅ OMe CH CH CH CHt-Bu Cl C₂F₅ OMe CH CH CH CH Et Cl C₂F₅ CN CH CH CH CH i-Pr Cl C₂F₅ CNCH CH CH CH t-Bu Cl C₂F₅ CN

[0353] TABLE 17

W X Y Z R³ R⁴ R⁷ R⁸ CH CH CH CH Et Me CF₃ Cl CH CH CH CH i-Pr Me CF₃ ClCH CH CH CH t-Bu Me CF₃ Cl CH CH CH CH Et Me CF₃ Br CH CH CH CH i-Pr MeCF₃ Br CH CH CH CH t-Bu Me CF₃ Br CH CH CH CH Et Me CF₃ I CH CH CH CHi-Pr Me CF₃ I CH CH CH CH t-Bu Me CF₃ I CH CH CH CH Et Me CF₃ F CH CH CHCH i-Pr Me CF₃ F CH CH CH CH t-Bu Me CF₃ F CH CH CH CH Et Me CF₃ Me CHCH CH CH i-Pr Me CF₃ Me CH CH CH CH t-Bu Me CF₃ Me CH CH CH CH Et Me CF₃CF₃ CH CH CH CH i-Pr Me CF₃ CF₃ CH CH CH CH t-Bu Me CF₃ CF₃ CH CH CH CHEt Me CF₃ OMe CH CH CH CH i-Pr Me CF₃ OMe CH CH CH CH t-Bu Me CF₃ OMe CHCH CH CH Et Me CF₃ CN CH CH CH CH i-Pr Me CF₃ CN CH CH CH CH t-Bu Me CF₃CN CH CH CH CH Et Cl CF₃ Cl CH CH CH CH i-Pr Cl CF₃ Cl CH CH CH CH t-BuCl CF₃ Cl CH CH CH CH Et Cl CF₃ Br CH CH CH CH i-Pr Cl CF₃ Br CH CH CHCH t-Bu Cl CF₃ Br CH CH CH CH Et Cl CF₃ I CH CH CH CH i-Pr Cl CF₃ I CHCH CH CH t-Bu Cl CF₃ I CH CH CH CH Et Cl CF₃ F CH CH CH CH i-Pr Cl CF₃ FCH CH CH CH t-Bu Cl CF₃ F CH CH CH CH Et Cl CF₃ Me CH CH CH CH i-Pr ClCF₃ Me CH CH CH CH t-Bu Cl CF₃ Me CH CH CH CH Et Cl CF₃ CF₃ CH CH CH CHi-Pr Cl CF₃ CF₃ CH CH CH CH t-Bu Cl CF₃ CF₃ CH CH CH CH Et Cl CF₃ OMe CHCH CH CH i-Pr Cl CF₃ OMe CH CH CH CH t-Bu Cl CF₃ OMe CH CH CH CH Et ClCF₃ CN CH CH CH CH i-Pr Cl CF₃ CN CH CH CH CH t-Bu Cl CF₃ CN CH CH CH NEt Me CF₃ Cl CH CH CH N i-Pr Me CF₃ Cl CH CH CH N t-Bu Me CF₃ Cl CH CHCH N Et Me CF₃ Br CH CH CH N i-Pr Me CF₃ Br CH CH CH N t-Bu Me CF₃ Br CHCH CH N Et Me CF₃ I CH CH CH N i-Pr Me CF₃ I CH CH CH N t-Bu Me CF₃ I CHCH CH N Et Me CF₃ F CH CH CH N i-Pr Me CF₃ F CH CH CH N t-Bu Me CF₃ F CHCH CH N Et Me CF₃ Me CH CH CH N i-Pr Me CF₃ Me CH CH CH N t-Bu Me CF₃ MeCH CH CH N Et Me CF₃ CF₃ CH CH CH N i-Pr Me CF₃ CF₃ CH CH CH N t-Bu MeCF₃ CF₃ CH CH CH N Et Me CF₃ OMe CH CH CH N i-Pr Me CF₃ OMe CH CH CH Nt-Bu Me CF₃ OMe CH CH CH N Et Me CF₃ CN CH CH CH N i-Pr Me CF₃ CN CH CHCH N t-Bu Me CF₃ CN CH CH CH N Et Cl CF₃ Cl CH CH CH N i-Pr Cl CF₃ Cl CHCH CH N t-Bu Cl CF₃ Cl CH CH CH N Et Cl CF₃ Br CH CH CH N i-Pr Cl CF₃ BrCH CH CH N t-Bu Cl CF₃ Br CH CH CH N Et Cl CF₃ I CH CH CH N i-Pr Cl CF₃I CH CH CH N t-Bu Cl CF₃ I CH CH CH N Et Cl CF₃ F CH CH CH N i-Pr Cl CF₃F CH CH CH N t-Bu Cl CF₃ F CH CH CH N Et Cl CF₃ Me CH CH CH N i-Pr ClCF₃ Me CH CH CH N t-Bu Cl CF₃ Me CH CH CH N Et Cl CF₃ CF₃ CH CH CH Ni-Pr Cl CF₃ CF₃ CH CH CH N t-Bu Cl CF₃ CF₃ CH CH CH N Et Cl CF₃ OMe CHCH CH N i-Pr Cl CF₃ OMe CH CH CH N t-Bu Cl CF₃ OMe CH CH CH N Et Cl CF₃CN CH CH CH N i-Pr Cl CF₃ CN CH CH CH N t-Bu Cl CF₃ CN CH CH N CH Et MeCF₃ Cl CH CH N CH i-Pr Me CF₃ Cl CH CH N CH t-Bu Me CF₃ Cl CH CH N CH EtMe CF₃ Br CH CH N CH i-Pr Me CF₃ Br CH CH N CH t-Bu Me CF₃ Br CH CH N CHEt Me CF₃ I CH CH N CH i-Pr Me CF₃ I CH CH N CH t-Bu Me CF₃ I CH CH N CHEt Me CF₃ F CH CH N CH i-Pr Me CF₃ F CH CH N CH t-Bu Me CF₃ F CH CH N CHEt Me CF₃ Me CH CH N CH i-Pr Me CF₃ Me CH CH N CH t-Bu Me CF₃ Me CH CH NCH Et Me CF₃ CF₃ CH CH N CH i-Pr Me CF₃ CF₃ CH CH N CH t-Bu Me CF₃ CF₃CH CH N CH Et Me CF₃ OMe CH CH N CH i-Pr Me CF₃ OMe CH CH N CH t-Bu MeCF₃ OMe CH CH N CH Et Me CF₃ CN CH CH N CH i-Pr Me CF₃ CN CH CH N CHt-Bu Me CF₃ CN CH CH N CH Et Cl CF₃ Cl CH CH N CH i-Pr Cl CF₃ Cl CH CH NCH t-Bu Cl CF₃ Cl CH CH N CH Et Cl CF₃ Br CH CH N CH i-Pr Cl CF₃ Br CHCH N CH t-Bu Cl CF₃ Br CH CH N CH Et Cl CF₃ I CH CH N CH i-Pr Cl CF₃ ICH CH N CH t-Bu Cl CF₃ I CH CH N CH Et Cl CF₃ F CH CH N CH i-Pr Cl CF₃ FCH CH N CH t-Bu Cl CF₃ F CH CH N CH Et Cl CF₃ Me CH CH N CH i-Pr Cl CF₃Me CH CH N CH t-Bu Cl CF₃ Me CH CH N CH Et Cl CF₃ CF₃ CH CH N CH i-Pr ClCF₃ CF₃ CH CH N CH t-Bu Cl CF₃ CF₃ CH CH N CH Et Cl CF₃ OMe CH CH N CHi-Pr Cl CF₃ OMe CH CH N CH t-Bu Cl CF₃ OMe CH CH N CH Et Cl CF₃ CN CH CHN CH i-Pr Cl CF₃ CN CH CH N CH t-Bu Cl CF₃ CN CH N CH CH Et Me CF₃ Cl CHN CH CH i-Pr Me CF₃ Cl CH N CH CH t-Bu Me CF₃ Cl CH N CH CH Et Me CF₃ BrCH N CH CH i-Pr Me CF₃ Br CH N CH CH t-Bu Me CF₃ Br CH N CH CH Et Me CF₃I CH N CH CH i-Pr Me CF₃ I CH N CH CH t-Bu Me CF₃ I CH N CH CH Et Me CF₃F CH N CH CH i-Pr Me CF₃ F CH N CH CH t-Bu Me CF₃ F CH N CH CH Et Me CF₃Me CH N CH CH i-Pr Me CF₃ Me CH N CH CH t-Bu Me CF₃ Me CH N CH CH Et MeCF₃ CF₃ CH N CH CH i-Pr Me CF₃ CF₃ CH N CH CH t-Bu Me CF₃ CF₃ CH N CH CHEt Me CF₃ OMe CH N CH CH i-Pr Me CF₃ OMe CH N CH CH t-Bu Me CF₃ OMe CH NCH CH Et Me CF₃ CN CH N CH CH i-Pr Me CF₃ CN CH N CH CH t-Bu Me CF₃ CNCH N CH CH Et Cl CF₃ Cl CH N CH CH i-Pr Cl CF₃ Cl CH N CH CH t-Bu Cl CF₃Cl CH N CH CH Et Cl CF₃ Br CH N CH CH i-Pr Cl CF₃ Br CH N CH CH t-Bu ClCF₃ Br CH N CH CH Et Cl CF₃ I CH N CH CH i-Pr Cl CF₃ I CH N CH CH t-BuCl CF₃ I CH N CH CH Et Cl CF₃ F CH N CH CH i-Pr Cl CF₃ F CH N CH CH t-BuCl CF₃ F CH N CH CH Et Cl CF₃ Me CH N CH CH i-Pr Cl CF₃ Me CH N CH CHt-Bu Cl CF₃ Me CH N CH CH Et Cl CF₃ CF₃ CH N CH CH i-Pr Cl CF₃ CF₃ CH NCH CH t-Bu Cl CF₃ CF₃ CH N CH CH Et Cl CF₃ OMe CH N CH CH i-Pr Cl CF₃OMe CH N CH CH t-Bu Cl CF₃ OMe CH N CH CH Et Cl CF₃ CN CH N CH CH i-PrCl CF₃ CN CH N CH CH t-Bu Cl CF₃ CN N CH CH CH Et Me CF₃ Cl N CH CH CHi-Pr Me CF₃ Cl N CH CH CH t-Bu Me CF₃ Cl N CH CH CH Et Me CF₃ Br N CH CHCH i-Pr Me CF₃ Br N CH CH CH t-Bu Me CF₃ Br N CH CH CH Et Me CF₃ I N CHCH CH i-Pr Me CF₃ I N CH CH CH t-Bu Me CF₃ I N CH CH CH Et Me CF₃ F N CHCH CH i-Pr Me CF₃ F N CH CH CH t-Bu Me CF₃ F N CH CH CH Et Me CF₃ Me NCH CH CH i-Pr Me CF₃ Me N CH CH CH t-Bu Me CF₃ Me N CH CH CH Et Me CF₃CF₃ N CH CH CH i-Pr Me CF₃ CF₃ N CH Cu CH t-Bu Me CF₃ CF₃ N CH CH CH EtMe CF₃ OMe N CH CH CH i-Pr Me CF₃ OMe N CH CH CH t-Bu Me CF₃ OMe N CH CHCH Et Me CF₃ CN N CH CH CH i-Pr Me CF₃ CN N CH CH CH t-Bu Me CF₃ CN N CHCH CH Et Cl CF₃ Cl N CH CH CH i-Pr Cl CF₃ Cl N CH CH CH t-Bu Cl CF₃ Cl NCH CH CH Et Cl CF₃ Br N CH CH CH i-Pr Cl CF₃ Br N CH CH CH t-Bu Cl CF₃Br N CH CH CH Et Cl CF₃ I N CH CH CH i-Pr Cl CF₃ I N CH CH CH t-Bu ClCF₃ I N CH CH CH Et Cl CF₃ F N CH CH CH i-Pr Cl CF₃ F N CH CH CH t-Bu ClCF₃ F N CH CH CH Et Cl CF₃ Me N CH CH CH i-Pr Cl CF₃ Me N CH CH CH t-BuCl CF₃ Me N CH CH CH Et Cl CF₃ CF₃ N CH CH CH i-Pr Cl CF₃ CF₃ N CH CH CHt-Bu Cl CF₃ CF₃ N CH CH CH Et Cl CF₃ OMe N CH CH CH i-Pr Cl CF₃ OMe N CHCH CH t-Bu Cl CF₃ OMe N CH CH CH Et Cl CF₃ CN N CH CH CH i-Pr Cl CF₃ CNN CH CH CH t-Bu Cl CF₃ CN CH N CH N Et Me CF₃ Cl CH N CH N i-Pr Me CF₃Cl CH N CH N t-Bu Me CF₃ Cl CH N CH N Et Me CF₃ Br CH N CH N i-Pr Me CF₃Br CH N CH N t-Bu Me CF₃ Br CH N CH N Et Me CF₃ I CH N CH N i-Pr Me CF₃I CH N CH N t-Bu Me CF₃ I CH N CH N Et Me CF₃ F CH N CH N i-Pr Me CF₃ FCH N CH N t-Bu Me CF₃ F CH N CH N Et Me CF₃ Me CH N CH N i-Pr Me CF₃ MeCH N CH N t-Bu Me CF₃ Me CH N CH N Et Me CF₃ CF₃ CH N CH N i-Pr Me CF₃CF₃ CH N CH N t-Bu Me CF₃ CF₃ CH N CH N Et Me CF₃ OMe CH N CH N i-Pr MeCF₃ OMe CH N CH N t-Bu Me CF₃ OMe CH N CH N Et Me CF₃ CN CH N CH N i-PrMe CF₃ CN CH N CH N t-Bu Me CF₃ CN CH N CH N Et Cl CF₃ Cl CH N CH N i-PrCl CF₃ Cl CH N CH N t-Bu Cl CF₃ Cl CH N CH N Et Cl CF₃ Br CH N CH N i-PrCl CF₃ Br CH N CH N t-Bu Cl CF₃ Br CH N CH N Et Cl CF₃ I CH N CH N i-PrCl CF₃ I CH N CH N t-Bu Cl CF₃ I CH N CH N Et Cl CF₃ F CH N CH N i-Pr ClCF₃ F CH N CH N t-Bu Cl CF₃ F CH N CH N Et Cl CF₃ Me CH N CH N i-Pr ClCF₃ Me CH N CH N t-Bu Cl CF₃ Me CH N CH N Et Cl CF₃ CF₃ CH N CH N i-PrCl CF₃ CF₃ CH N CH N t-Bu Cl CF₃ CF₃ CH N CH N Et Cl CF₃ OMe CH N CH Ni-Pr Cl CF₃ OMe CH N CH N t-Bu Cl CF₃ OMe CH N CH N Et Cl CF₃ CN CH N CHN i-Pr Cl CF₃ CN CH N CH N t-Bu Cl CF₃ CN CH CH CH CCl Et Me CF₃ Cl CHCH CH CCl i-Pr Me CF₃ Cl CH CH CH CCl t-Bu Me CF₃ Cl CH CH CH CCl Et MeCF₃ Br CH CH CH CCl i-Pr Me CF₃ Br CH CH CH CCl t-Bu Me CF₃ Br CH CH CHCCl Et Me CF₃ I CH CH CH CCl i-Pr Me CF₃ I CH CH CH CCl t-Bu Me CF₃ I CHCH CH CCl Et Me CF₃ F CH CH CH CCl i-Pr Me CF₃ F CH CH CH CCl t-Bu MeCF₃ F CH CH CH CCl Et Me CF₃ Me CH CH CH CCl i-Pr Me CF₃ Me CH CH CH CClt-Bu Me CF₃ Me CH CH CH CCl Et Me CF₃ CF₃ CH CH CH CCl i-Pr Me CF₃ CF₃CH CH CH CCl t-Bu Me CF₃ CF₃ CH CH CH CCl Et Me CF₃ OMe CH CH CH CCli-Pr Me CF₃ OMe CH CH CH CCl t-Bu Me CF₃ OMe CH CH CH CCl Et Me CF₃ CNCH CH CH CCl i-Pr Me CF₃ CN CH CH CH CCl t-Bu Me CF₃ CN CH CH CH CCl EtCl CF₃ Cl CH CH CH CCl i-Pr Cl CF₃ Cl CH CH CH CCl t-Bu Cl CF₃ Cl CH CHCH CCl Et Cl CF₃ Br CH CH CH CCl i-Pr Cl CF₃ Br CH CH CH CCl t-Bu Cl CF₃Br CH CH CH CCl Et Cl CF₃ I CH CH CH CCl i-Pr Cl CF₃ I CH CH CH CCl t-BuCl CF₃ I CH CH CH CCl Et Cl CF₃ F CH CH CH CCl i-Pr Cl CF₃ F CH CH CHCCl t-Bu Cl CF₃ F CH CH CH CCl Et Cl CF₃ Me CH CH CH CCl i-Pr Cl CF₃ MeCH CH CH CCl t-Bu Cl CF₃ Me CH CH CH CCl Et Cl CF₃ CF₃ CH CH CH CCl i-PrCl CF₃ CF₃ CH CH CH CCl t-Bu Cl CF₃ CF₃ CH CH CH CCl Et Cl CF₃ OMe CH CHCH CCl i-Pr Cl CF₃ OMe CH CH CH CCl t-Bu Cl CF₃ OMe CH CH CH CCl Et ClCF₃ CN CH CH CH CCl i-Pr Cl CF₃ CN CH CH CH CCl t-Bu Cl CF₃ CN CH CH CHCF Et Me CF₃ Cl CH CH CH CF i-Pr Me CF₃ Cl CH CH CH CF t-Bu Me CF₃ Cl CHCH CH CF Et Me CF₃ Br CH CH CH CF i-Pr Me CF₃ Br CH CH CH CF t-Bu Me CF₃Br CH CH CH CF Et Me CF₃ I CH CH CH CF i-Pr Me CF₃ I CH CH CH CF t-Bu MeCF₃ I CH CH CH CF Et Me CF₃ F CH CH CH CF i-Pr Me CF₃ F CH CH CH CF t-BuMe CF₃ F CH CH CH CF Et Me CF₃ Me CH CH CH CF i-Pr Me CF₃ Me CH CH CH CFt-Bu Me CF₃ Me CH CH CH CF Et Me CF₃ CF₃ CH CH CH CF i-Pr Me CF₃ CF₃ CHCH CH CF t-Bu Me CF₃ CF₃ CH CH CH CF Et Me CF₃ OMe CH CH CH CF i-Pr MeCF₃ OMe CH CH CH CF t-Bu Me CF₃ OMe CH CH CH CF Et Me CF₃ CN CH CH CH CFi-Pr Me CF₃ CN CH CH CH CF t-Bu Me CF₃ CN CH CH CH CF Et Cl CF₃ Cl CH CHCH CF i-Pr Cl CF₃ Cl CH CH CH CF t-Bu Cl CF₃ Cl CH CH CH CF Et Cl CF₃ BrCH CH CH CF i-Pr Cl CF₃ Br CH CH CH CF t-Bu Cl CF₃ Br CH CH CH CF Et ClCF₃ I CH CH CH CF i-Pr Cl CF₃ I CH CH CH CF t-Bu Cl CF₃ I CH CH CH CFi-Pr Cl CF₃ F CH CH CH CF t-Bu Cl CF₃ F CH CH CH CF Et Cl CF₃ Me CH CHCH CF i-Pr Cl CF₃ Me CH CH CH CF t-Bu Cl CF₃ Me CH CH CH CF Et Cl CF₃CF₃ CH CH CH CF i-Pr Cl CF₃ CF₃ CH CH CH CF t-Bu Cl CF₃ CF₃ CH CH CH CFEt Cl CF₃ OMe CH CH CH CF i-Pr Cl CF₃ OMe CH CH CH CF t-Bu Cl CF₃ OMe CHCH CH CF Et Cl CF₃ CN CH CH CH CF i-Pr Cl CF₃ CN CH CH CH CF t-Bu Cl CF₃CN CH CH CH CH Et Me C₂F₅ Cl CH CH CH CH i-Pr Me C₂F₅ Cl CH CH CH CHt-Bu Me C₂F₅ Cl CH CH CH CH Et Me C₂F₅ Br CH CH CH CH i-Pr Me C₂F₅ Br CHCH CH CH t-Bu Me C₂F₅ Br CH CH CH CH Et Me C₂F₅ I CH CH CH CH i-Pr MeC₂F₅ I CH CH CH CH t-Bu Me C₂F₅ I CH CH CH CH Et Me C₂F₅ F CH CH CH CHi-Pr Me C₂F₅ F CH CH CH CH t-Bu Me C₂F₅ F CH CH CH CH Et Me C₂F₅ Me CHCH CH CH i-Pr Me C₂F₅ Me CH CH CH CH t-Bu Me C₂F₅ Me CH CH CH CH Et MeC₂F₅ CF₃ CH CH CH CH i-Pr Me C₂F₅ CF₃ CH CH CH CH t-Bu Me C₂F₅ CF₃ CH CHCH CH Et Me C₂F₅ OMe CH CH CH CH i-Pr Me C₂F₅ OMe CH CH CH CH t-Bu MeC₂F₅ OMe CH CH CH CH Et Me C₂F₅ CN CH CH CH CH i-Pr Me C₂F₅ CN CH CH CHCH t-Bu Me C₂F₅ CN CH CH CH CH Et Cl C₂F₅ Cl CH CH CH CH i-Pr Cl C₂F₅ ClCH CH CH CH t-Bu Cl C₂F₅ Cl CH CH CH CH Et Cl C₂F₅ Br CH CH CH CH i-PrCl C₂F₅ Br CH CH CH CH t-Bu Cl C₂F₅ Br CH CH CH CH Et Cl C₂F₅ I CH CH CHCH i-Pr Cl C₂F₅ I CH CH CH CH t-Bu Cl C₂F₅ I CH CH CH CH Et Cl C₂F₅ F CHCH CH CH i-Pr Cl C₂F₅ F CH CH CH CH t-Bu Cl C₂F₅ F CH CH CH CH Et ClC₂F₅ Me CH CH CH CH i-Pr Cl C₂F₅ Me CH CH CH CH t-Bu Cl C₂F₅ Me CH CH CHCH Et Cl C₂F₅ CF₃ CH CH CH CH i-Pr Cl C₂F₅ CF₃ CH CH CH CH t-Bu Cl C₂F₅CF₃ CH CH CH CH Et Cl C₂F₅ OMe CH CH CH CH i-Pr Cl C₂F₅ OMe CH CH CH CHt-Bu Cl C₂F₅ OMe CH CH CH CH Et Cl C₂F₅ CN CH CH CH CH i-Pr Cl C₂F₅ CNCH CH CH CH t-Bu Cl C₂F₅ CN

[0354] Formulation/Utility

[0355] Compounds of this invention will generally be used as aformulation or composition with an agriculturally suitable carriercomprising at least one of a liquid diluent, a solid diluent or asurfactant. The formulation or composition ingredients are selected tobe consistent with the physical properties of the active ingredient,mode of application and environmental factors such as soil type,moisture and temperature. Useful formulations include liquids such assolutions (including emulsifiable concentrates), suspensions, emulsions(including microemulsions and/or suspoemulsions) and the like whichoptionally can be thickened into gels. Useful formulations furtherinclude solids such as dusts, powders, granules, pellets, tablets,films, and the like which can be water-dispersible (“wettable”) orwater-soluble. Active ingredient can be (micro)encapsulated and furtherformed into a suspension or solid formulation; alternatively the entireformulation of active ingredient can be encapsulated (or “overcoated”).Encapsulation can control or delay release of the active ingredient.Sprayable formulations can be extended in suitable media and used atspray volumes from about one to several hundred liters per hectare.High-strength compositions are primarily used as intermediates forfurther formulation.

[0356] The formulations will typically-contain effective amounts ofactive ingredient, diluent and surfactant within the followingapproximate ranges that add up to 100 percent by weight. Weight PercentActive Ingredient Diluent Surfactant Water-Dispersible and Water- 5-900-94 1-15 soluble Granules, Tablets and Powders. Suspensions, Emulsions,5-50 40-95  0-15 Solutions (including Emulsifiable Concentrates) Dusts1-25 70-99  0-5  Granules and Pellets 0.01-99     5-99.99 0-15 HighStrength Compositions 90-99  0-10 0-2 

[0357] Typical solid diluents are described in Watkins, et al., Handbookof Insecticide Dust Diluents and Carriers, 2nd Ed., Dorland Books,Caldwell, N.J. Typical liquid diluents are described in Marsden,Solvents Guide, 2nd Ed., Interscience, New York, 1950. McCutcheon'sDetergents and Emulsifiers Annual, Allured Publ. Corp., Ridgewood, N.J.,as well as Sisely and Wood, Encyclopedia of Surface Active Agents,Chemical Publ. Co., Inc., New York, 1964, list surfactants andrecommended uses. All formulations can contain minor amounts ofadditives to reduce foam, caking, corrosion, microbiological growth andthe like, or thickeners to increase viscosity.

[0358] Surfactants include, for example, polyethoxylated alcohols,polyethoxylated alkylphenols, polyethoxylated sorbitan fatty acidesters, dialkyl sulfosuccinates, alkyl sulfates, alkylbenzenesulfonates, organosilicones, N,N-dialkyltaurates, lignin sulfonates,naphthalene sulfonate formaldehyde condensates, polycarboxylates, andpolyoxyethylene/polyoxypropylene block copolymers. Solid diluentsinclude, for example, clays such as bentonite, montmoriflonite,attapulgite and kaolin, starch, sugar, silica, talc, diatomaceous earth,urea, calcium carbonate, sodium carbonate and bicarbonate, and sodiumsulfate. Liquid diluents include, for example, water,N,N-dimethylformamide, dimethyl sulfoxide, N-alkylpyrrolidone, ethyleneglycol, polypropylene glycol, paraffins, alkylbenzenes,alkcylnaphthalenes, oils of olive, castor, linseed, tung, sesame, corn,peanut, cotton-seed, soybean, rape-seed and coconut, fatty acid esters,ketones such as cyclohexanone, 2-heptanone, isophorone and4-hydroxy-4methyl-2-pentanone, and alcohols such as methanol,cyclohexanol, decanol and tetrahydrofurfuryl alcohol.

[0359] Solutions, including emulsifiable concentrates, can be preparedby simply mixing the ingredients. Dusts and powders can be prepared byblending and, usually, grinding as in a hammer mill or fluid-energymill. Suspensions are usually prepared by wet-milling; see, for example,U.S. Pat. No. 3,060,084. Granules and pellets can be prepared byspraying the active material upon preformed granular carriers or byagglomeration techniques. See Browning, “Agglomeration”, ChemicalEngineering, Dec. 4, 1967, pp 147-48, Perry's Chemical Engineer'sHandbook, 4th Ed., McGraw-Hill, New York, 1963, pages 8-57 andfollowing, and WO 91/13546. Pellets can be prepared as described in U.S.Pat. No. 4,172,714. Water-dispersible and water-soluble granules can beprepared as taught in U.S. Pat. No. 4,144,050, U.S. Pat. No. 3,920,442and DE 3,246,493. Tablets can be prepared as taught in U.S. Pat No.5,180,587, U.S. Pat. No. 5,232,701 and U.S. Pat. No. 5,208,030. Filmscan be prepared as taught in GB 2,095,558 and U.S. Pat. No. 3,299,566.

[0360] For further information regarding the art of formulation, seeU.S. Pat. No. 3,235,361, Col. 6, line 16 through Col. 7, line 19 andExamples 1041; U.S. Pat. No. 3,309,192, Col. 5, line 43 through Col. 7,line 62 and Examples 8, 12, 15, 39, 41, 52, 53, 58, 132, 138-140,162-164, 166, 167 and 169-182; U.S. Pat No. 2,891,855, Col. 3, line 66through Col. 5, line 17 and Examples 1-4; Klingman, Weed Control as aScience, John Wiley and Sons, Inc., New York, 1961, pp 81-96; and Hanceet al., Weed Control Handbook, 8th Ed., Blackwell ScientificPublications, Oxford, 1989.

[0361] In the following Examples, all percentages are by weight and allformulations are prepared in conventional ways. Compound numbers referto compounds in Index Tables A. Example A Wettable Powder Compound 165.0% dodecylphenol polyethylene glycol ether  2.0% sodiumligninsulfonate  4.0% sodium silicoaluminate  6.0% montmorillonite(calcined)  23.0%. Example B Granule Compound 1 10.0% attapulgitegranules (low volatile matter,  90.0%. 0.71/0.30 mm; U.S.S. No. 25-50sieves) Example C Extruded Pellet Compound 1 25.0% anhydrous sodiumsulfate 10.0% crude calcium ligninsulfonate  5.0% sodiumalkylnaphthalenesulfonate  1.0% calcium/magnesium bentonite  59.0%.Example D Emulsifiable Concentrate Compound 1 20.0% blend of oil solublesulfonates 10.0% and polyoxyethylene ethers isophorone  70.0%.

[0362] The compounds of this invention exhibit activity against a widespectrum of foliar-feeding, fruit-feeding, stem or root feeding,seed-feeding, aquatic and soil-inhabiting arthropods (term “arthropods”includes insects, mites and nematodes) which are pests of growing andstored agronomic crops, forestry, greenhouse crops, ornamentals, nurserycrops, stored food and fiber products, livestock, household, and publicand animal health. Those skilled in the art will appreciate that not allcompounds are equally effective against all growth stages of all pests.Nevertheless, all of the compounds of this invention display activityagainst pests that include: eggs, larvae and adults of the OrderLepidoptera; eggs, foliar-feeding, fruit-feeding, root-feeding,seed-feeding larvae and adults of the Order Coleoptera; eggs, immaturesand adults of the Orders Hemiptera and Homoptera; eggs, larvae, nymphsand adults of the Order Acari; eggs, immatures and adults of the OrdersThysanoptera, Orthoptera and Dermaptera; eggs, immatures and adults ofthe Order Diptera; and eggs, juveniles and adults of the PhylumNematoda. The compounds of this invention are also active against pestsof the Orders Hymenoptera, Isoptera, Siphonaptera, Blattaria, Thysanuraand Psocoptera; pests belonging to the Class Arachnida and PhylumPlatyhelminthes. Specifically, the compounds are active against southerncorn rootworm (Diabrotica undecimpunctata howardi), aster lealhopper(Mascrosteles fascifrons), boll weevil (Anthonomus grandis), two-spottedspider mite (Tetranychus urticae), fall armyworm (Spodopterafrugiperda), black bean aphid (Aphis fabae), green peach aphid (Myzuspersica), cotton aphid (Aphis gossypii), Russian wheat aphid (Diuraphisnoxia), English grain aphid (Sitobion avenae), whitefly (Bemisiatabacii), tobacco budworm (Heliothis virescens), rice water weevil(Lissorhoptrus oryzophilus), rice leaf beetle (Oulema oryzae),whitebacked planthopper (Sogatella furcifera), green leafhopper(Nephotettix cincticeps), brown planthopper (Nilaparvata lugens), smallbrown planthopper (Laodelphax striatellus), rice stem borer (Chilosuppressalis), rice leafroller (Cnaphalocrocis medinalis), black ricestink bug (Scotinophara lurida), rice stink bug (Oebalus pugnax), ricebug (Leptocorisa chinensis), slender rice bug (Cletus puntiger),southern green stink bug (Nezara viridula) and german cockroach(Blatella germanica). The compounds are active on mites, demonstratingovicidal, larvicidal and chemosterilant activity against such familiesas Tetranychidae including Tetranychus urticae, Tetranychuscinnabarinus, Tetranychus mcdanieli, Tetranychus pacificus, Tetranychusturkestani, Byrobia rubrioculus, Panonychus ulmi, Panonychus citri,Eotetranychus carpini borealis, Eotetranychus, hicoriae, Eotetranychussexmaculatus, Eotetranychusyumensis, Eotetranychus banksi andOligonychus pratensis; Tenuipalpidae including Brevipalpus lewisi,Brevipalpusphoenicis, Brevipalpus californicus and Brevipalpus obovatus;Eriophyidae including Phyllocoptruta oleivora, Eriophyes sheldoni,Aculus cornutus, Epitrimerus pyri and Eriophyes mangiferae. See WO90/10623 and WO 92/00673 for more detailed pest descriptions.

[0363] Compounds of this invention can also be mixed with one or moreother insecticides, fungicides, nematocides, bactericides, acaricides,growth regulators, chemosterilants, semiochemicals, repellents,attractants, pheromones, feeding stimulants or other biologically activecompounds to form a multi-component pesticide giving an even broaderspectrum of agricultural protection. Examples of such agriculturalprotectants with which compounds of this invention can be formulatedare: insecticides such as abamectin, acephate, avermectin,azinphos-methyl, bifenthrin, buprofezin, carbofuran, chlorfenapyr,chlorpyrifos, chlorpyrifos-methyl, clothianidin, cyfluthrin,beta-cyfluthrin, cyhalothrin, lambda-cyhalothrin, cypermethrin,deltamethrin, diafenthiuron, diazinon, diflubenzuron, dimethoate,diofenolan, emamectin, endosulfan, esfenvalerate, fenothicarb,fenoxycarb, fenpropathrin, fenvalerate, fipronil, flucythrinate,tau-fluvalinate, flufenoxuron, fonophos, imidacloprid, isofenphos,malathion, metaldehyde, methamidophos, methidathion, methomyl,methonrene, methoxychlor, methyl7-chloro-2,5-dihydro-2-[[N-(methoxycarbonyl)-N-[4-(trifluoromethoxy)phenylamino]carbonyl]indeno[1,2-e][1,3,4]oxadiazine-4a(3H)-carboxylate(indoxacarb), monocrotophos, oxamyl, parathion, parathion-methyl,permetbrin, phorate, phosalone, phosmet, phosphamidon, pirimicarb,profenofos, pymetrozine, pyriproxyphen, rotenone, spionsad, suiprofos,tebufenozide, tefluthrin, terbufos, tetrachlorvinphos, thiacloprid,thiodicarb, tralomethrin, trichlorfon and triflumuron; fungicides suchas acibenzolar, azoxystrobin, benomyl, blasticidin-S, Bordeaux mixture(Tribasic copper sulfate), bromuconazole, carpropamid (KTU 3616),captafol, captan, carbendazim, chloroneb, chlorothalonil, copperoxychloride, copper salts, cymoxanil, cyproconazole, cyprodinil (CGA219417),(S)-3,5-dichloro-N-(3-chloro-1-ethyl-1-methyl-2-oxopropyl)-4-methylbenzamide(RH 7281), diclocymet (S-2900), diclomezine, dicloran,difenoconazole,(S)-3,5-dihydro-5-methyl-2-(methylthio)-5-phenyl-3-(phenylamino)-4H-imidazol-4-one(RP 407213), dimethomorph, diniconazole, diniconazole-M, dodine,edifenphos, epoxiconazole (BAS 480F), famoxadone, fenamidone, fenarimol,fenbuconazole, fencaramid (SZX0722), fenpiclonil, fenpropidin,fenpropimorph, fentin acetate, fentin hydroxide, fluazinam, fludioxonil,flumetover (RPA 403397), fluquinconazole, flusilazole, flutolanil,flutriafol, folpet, fosetyl-aluminum, furalaxyl, furametapyr (S-82658),hexaconazole, ipconazole, iprobenfos, iprodione, isoprothiolane,kasugamycin, kresoxim-methyl, mancozeb, maneb, mefenoxam, mepronil,metalaxyl, metconazole, metominiostrobin/fenominostrobin (SSF-126),myclobutanil, neo-asozin (ferric methanearsonate), oxadixyl,penconazole, pencycuron, probenazole, prochloraz, propamocarb,propiconazole, pyrifenox, pyraclostrobin, pyrimethanil, pyroquilon,quinoxyfen, spiroxamine, sulfur, tebuconazole, tetraconazole,thiabendazole, thifuzamide, thiophanate-methyl, thiram, triadimefon,triadimenol, tricyclazole, trifloxystrobin, triticonazole, validamycinand vinclozolin; nematocides such as aldicarb, oxamyl and fenamiphos;bactericides such as streptomycin; acaricides such as amitraz,chinomethionat, chlorobenzilate, cyhexatin, dicofol, dienochlor,etoxazole, fenazaquin, fenbutatin oxide, fenpropatlrin, fenpyroximate,hexythiazox, propargite, pyridaben and tebufenpyrad, and biologicalagents such as Bacillus thuringiensis, Bacillus thuringiensis deltaendotoxin, baculovirus, and entomopathogenic bacteria, virus and fungi.

[0364] Preferred insecticides and acaricides for mixing with compoundsof this invention include pyrethroids such as cypermethrin, cyhalothrin,cyfluthrin and beta-cyfluthrin, esfenvalerate, fenvalerate andtralomethrin; carbamates such as fenothicarb, methomyl, oxamyl andthiodicarb; neonicotinoids such as clothianidin, imidacloprid andthiacloprid, neuronal sodium channel blockers such as indoxacarb,insecticidal macrocyclic lactones such as spinosad, abamectin,avermectin and emamectin; GABA antagonists such as endosulfan andfipronil; insecticidal ureas such as flufenoxuron and trirlumuron,juvenile hormone mimics such as diofenolan and pyriproxyphen;pymetrozine; and amitraz. Preferred biological agents for mixing withcompounds of this invention include Bacillus thuringiensis and Bacillusthuringiensis delta endotoxin.

[0365] Most preferred mixtures include a mixture of a compound of thisinvention with cyhalothrin; a mixture of a compound of this inventionwith beta-cyfluthrin; a mixture of a compound of this invention withesfenvalerate; a mixture of a compound of this invention with methomyl;a mixture of a compound of this invention with imidacloprid; a mixtureof a compound of this invention with thiacloprid; a mixture of acompound of this invention with indoxacarb; a mixture of a compound ofthis invention with abamectin; a mixture of a compound of this inventionwith endosulfan; a mixture of a compound of this invention withfipronil; a mixture of a compound of this invention with flufenoxuron; amixture of a compound of this invention with pyriproxyphen; a mixture ofa compound of this invention with; a mixture of a compound of thisinvention with pymetrozine; a mixture of a compound of this inventionwith amitraz; a mixture of a compound of this invention with Bacillusthuringiensis and a mixture of a compound of this invention withBacillus thuringiensis delta endotoxin.

[0366] In certain instances, combinations with other arthropodicideshaving a similar spectrum of control but a different mode of action willbe particularly advantageous for resistance management.

[0367] Arthropod pests are controlled and protection of agronomic,horticultural and specialty crops, animal and human health is achievedby applying one or more of the compounds of this invention, in aneffective amount, to the environment of the pests including theagronomic and/or nonagronomic locus of infestation, to the area to beprotected, or directly on the pests to be controlled. Thus, the presentinvention further comprises a method for the control of foliar and soilinhabiting arthropods and nematode pests and protection of agronomicand/or nonagronomic crops, comprising applying one or more of thecompounds of the invention, or compositions containing at least one suchcompound, in an effective amount, to the environment of the pestsincluding the agronomic and/or nonagronomic locus of infestation, to thearea to be protected, or directly on the pests to be controlled. Apreferred method of application is by spraying. Alternatively, granularformulations of these compounds can be applied to the plant foliage orthe soil. Other methods of application include direct and residualsprays, aerial sprays, seed coats, microencapsulations, systemic uptake,baits, eartags, boluses, foggers, fumigants, aerosols, dusts and manyothers. The compounds can be incorporated into baits that are consumedby the arthropods or in devices such as traps and the like.

[0368] The compounds of this invention can be applied in their purestate, but most often application will be of a formulation comprisingone or more compounds with suitable carriers, diluents, and surfactantsand possibly in combination with a food depending on the contemplatedend use. A preferred method of application involves spraying a waterdispersion or refined oil solution of the compounds. Combinations withspray oils, spray oil concentrations, spreader stickers, adjuvants,other solvents, and synergists such as piperonyl butoxide often enhancecompound efficacy.

[0369] The rate of application required for effective control willdepend on such factors as the species of arthropod to be controlled, thepest's life cycle, life stage, its size, location, time of year, hostcrop or animal, feeding behavior, mating behavior, ambient moisture,temperature, and the like. Under normal circumstances, application ratesof about 0.01 to 2 kg of active ingredient per hectare are sufficient tocontrol pests in agronomic ecosystems, but as little as 0.001 kg/hectaremay be sufficient or as much as 8 kg/hectare may be required. Fornonagronomic applications, effective use rates will range from about 1.0to 50 mg/square meter but as little as 0.1 mg/square meter may besufficient or as much as 150 mg/square meter may be required.

[0370] The following TEST demonstrates the control efficacy of compoundsof this invention on specific pests. “Control efficacy” representsinhibition of arthropod development (including mortality) that causessignificantly reduced feeding. The pest control protection afforded bythe compounds is not limited, however, to these species. See IndexTables A through Q for compound descriptions. The followingabbreviations are used in the Index Tables which follow: t is tertiary,n is normal, i is iso, c is cyclo, s is secondary, Me is methyl, Et isethyl, Pr is propyl, i-Pr is isopropyl, c-Pr is cyclopropyl, Bu isbutyl, s-Bu is secondary butyl, Pent is pentyl, OMe is methoxy, OEt isethoxy, SMe is methylthio, SEt is ethylthio, CN is cyano, NO₂ is nitro,and Het is heterocycle. The abbreviation “Ex.” stands for “Example” andis followed by a number indicating in which example the compound isprepared. INDEX TABLE A

B is O, except where indicated Compound R¹ R² R³ R⁴ R⁵ and/or R⁶ m.p. °C. 1 (Ex 1) H i-Pr H 2-Me 4-OCF₃ 207-209 2 H i-Pr H 5-Cl 2-CF₃ 195-196 3H i-Pr H 5-Cl 2-Me-4-CF₃ 182-184 4 H i-Pr H 2-Me 4-CF₃ 238-240 5 H i-PrH 2-Me 4-CO₂Me 216-217 6 H i-Pr H 2-Me 3-NO₂ 230-233 7 H i-Pr H 2-Me3-CF₃-4-F 223-225 8 H i-Pr H 2-Me 3-CN 237-239 9 H i-Pr H 2-Me 2-OCF₃191-193 10 H t-Bu H 2-Me 4-OCF₃ 163-167 11 H t-Bu H 2-Me 4-CO₂Me 164-16912 H i-Pr H 2-Cl 4-CO₂Me 224-225 13 H t-Bu H 2-Me 2-OCF₃ 203-204 14 Ht-Bu H 2-Me 3-NO₂ 193-195 15 H t-Bu H 2-Me 3-CF₃-4-F 198-199 16 H i-Pr H2-OMe 4-OCF₃ 178-181 17 H i-Pr H 2-Me 2-OCF₃ 170-172 18 H i-Pr H 2-OMe3-CF₃-4-F 209-211 19 H i-Pr H 2-Cl 4-OCF₃ 215-216 20 H i-Pr Me 2-Me2-OCF₃ 153-155 21 H i-Pr H 5-Me 4-OCF₃ 173-175 22 H i-Pr H 5-Me 2-OCF₃180-185 23 H i-Pr H 5-Me 4-CO₂Me 182-184 24 H i-Pr Me 2-Me 4-OCF₃ Glass25 H i-Pr Me 2-Me 4-CO₂Me 67-73 26 H (1,2-di-Me)-Pr H 2-Me 4-OCF₃189-191 27 H CH(CH₃)CH₂OCH₃ H 2-Me 4-OCF₃ 147-148 28 H CH₂CH₂OCH₃ H 2-Me4-OCF₃ 153-155 29 H 2-Pent H 2-Me 4-OCF₃ 165-168 30 H s-Bu H 2-Me 4-OCF₃181-183 31 H propargyl H 2-Me 4-OCF₃ 190-192 32 H n-Pr H 2-Me 4-OCF₃189-191 33 H allyl H 2-Me 4-OCF₃ 185-187 34 H Me₂NCH₂CH₂ H 2-Me 4-OCF₃168-170 35 H propargyl H 2-Me 4-OCF₃ 202-204 36 H i-Bu H 2-Me 4-OCF₃182-183 37 H i-Pr H 2,4-di-Me 4-OCF₃ 205-208 38 H i-Pr H 2,4-di-Me4-CF₃ >230 39 H i-Pr H 2,4-di-Me 2-OCF₃ 231-232 40 H i-Pr H 2,4-di-Me4-CO₂Me 219-221 41 H i-Pr H 2,4-di-Me 3-CF₃-4-F 222-224 42 H t-Bu H2-OMe 4-CF₃ 210-214 43 H t-Bu H 2-OMe 4-OCF₃ 170-173 44 H i-Pr Me 2-Me3-NO₂ Oil 45 H i-Pr H 2-Cl 4-OCF₃ 187-194 46 H t-Bu H 2-Cl 4-OCF₃205-207 47 H allyl H 2-Cl 4-OCF₃ 188-189 48 H s-Bu H 2-Cl 4-OCF₃ 192-19349 H —CH₂CH₂CH₂CH₂— 2-Me 4-OCF₃ 138-142 50 H CH₂CF₃ H 2-Me 4-OCF₃ >23051 H c-Bu H 2-Me 4-OCF₃ 218-220 52 (Ex 3) H i-Pr H 2-Me 2-Me-4-CF₃247-248 53 H i-Pr H 5-Me 2-Me-4-CF₃ 186-188 54 H i-Pr H H 4-OCF₃ 185-18755 H i-Pr H H 3-NO₂ 199-200 56 H i-Pr H H 2-OCF₃ 118-122 57 Me i-Pr H H4-OCF₃ 117-118 58 Me i-Pr H H 3-NO₂ 134-136 59 Me i-Pr H H 2-OCF₃128-130 60 H i-Pr H H 3-CF₃ 176-177 61 H i-Pr H H 2-Me-4-CF₃ 100-106 62H Me H 2-Me 4-OCF₃ 204-206 63 H Et H 2-Me 4-OCF₃ 198-200 64 H NHi-Pr H2-Me 4-OCF₃ 126-128 65 H i-Pr H 2-Me 3-CF₃ 198-200 66 H i-Pr H 2-Me4-CN >230 67 H i-Pr H 2-Me 2-NO₂ >230 68 H i-Pr H 2-Me 3,5-di-CF₃ >23069 H i-Pr H 2-Me 4-NO₂ 227-230 70 H i-Pr H 2-Me 2-CF₃ 227-230 71 H i-PrH H 2-Me-4-OCF₃ 118-124 72 H i-Pr H H 4-CF₃ 196-198 73 H i-Pr H 2-Me2-Me-4-SCF₂H 212-213 74 H t-Bu H 2-Me 2-Me-4-SCF₂H 193-195 75 H i-Pr H2-Me 2-Me-4-OCF₃ 221-222 76 H t-Bu H 2-Me 4-CF₃ 217-219 77 H t-Bu H 2-Me3-CF₃ 197-198 78 H t-Bu H 2-Me 3,5-di-CF₃ 206-207 79 H t-Bu H 2-Me4-CN >230 80 H t-Bu H 2-Me 4-NO₂ >230 81 Me i-Pr H 2-Me 2-CF₃ oil 82 Mei-Pr H 2-Me 4-OCF₃ 151-157 83 Me i-Pr H H 2-Me-4-OCF₃ 103-107 84 Me t-BuH 2-Me 2-Me-4-CF₃ 233-234 85 H t-Bu H 2-Me 2-Me-4-OCF₃ 207-209 86 H t-BuH 2-Me 2,5-di-CF₃ 199-201 87 H i-Pr H 2-CF3 4-OCF₃ 183-185 88 H i-Pr H2-CF3 4-CF₃ 211-212 89 H t-Bu H 2-CF₃ 4-CF₃ 191-192 90 H R-(−)-s-Bu H2-Me 4-OCF₃ 170-172 91 H S-(+)-s-Bu H 2-Me 4-OCF₃ 177-179 92 Me i-Pr H H4-CF₃ oil 93 Me i-Pr H 2-OCF₂H 4-OCF₃ 162-164 94 H t-Bu H 2-CF₃ 4-OCF₃145-148 95 H i-Pr Me 2-CF₃ 4-CF₃ 151-154 96 H i-Pr Me 2-CF₃ 4-OCF₃140-144 97 H i-Pr H 2-OCF₂H 4-CF₃ 224-227 98 H i-Pr H 2,4-di-Me2-Me-4-CF₃ >230 99 H i-Pr H 2-Cl 2-Me-4-CF₃ >230 100 H CH(CH₃)CH₂OCH₃ H2-Cl 2-Me-4-CF₃ 194-197 101 H s-Bu H 2-Cl 2-Me-4-CF₃ 212-214 102 H c-PrH 2-Me 4-OCF₃ 208-210 103 H CH(CH₃)CH₂OCH₃ H 2,4-di-Me 4-OCF₃ 166-168104 H CH(CH₃)CH₂OCH₃ H 2,4-di-Me 4-CF₃ 192-194 105 H i-Pr H 4-Me 4-CF₃212-213 106 H i-Pr H 4-Me 4-OCF₃ 204-205 107 H i-Pr H 2-Br-4-Me4-OCF₃ >230 108 H t-Bu H 2-Br-4-Me 4-OCF₃ 118-120 109 H i-Pr H 2-NO₂4-CF₃ 203-204 110 H t-Bu H 2-NO₂ 4-CF₃ 199-200 111 H i-Pr H 2-NO₂ 4-OCF₃204-205 112 H t-Bu H 2-NO₂ 4-OCF₃ 181-183 113 H i-Pr H 2-Me2-Me-4-S(O)₂CF₂H 218-221 114 H i-Pr H 2-Me 2-Me-4-S(O)CF₂H 203-206 115 HCH(CH₃)CH₂OCH₃ H 3-Cl 4-CF₃ 158-161 116 H i-Pr H 4-Br 4-CF₃ 232-234 117H t-Bu H 4-Br 4-CF₃ 204-206 118 H CH(CH₃)CH₂OCH₃ H 4-Br 4-CF₃ 157-158119 H i-Pr H 4-Br 4-OCF₃ 221-222 120 H t-Bu H 4-Br 4-OCF₃ 173-175 121 HCH(CH₃)CH₂OCH₃ H 4-Br 4-OCF₃ 153-155 122 H CH(CH₃)CH₂OCH₃ H 3-Cl 4-OCF₃137-140 123 H i-Pr H 4-F 4-CF₃ 205-206 124 H t-Bu H 2-Cl 2-Me-4-CF₃237-240 125 H 2-Pent H 2-Me 4-CF₃ 194-196 126 H s-Bu H 2-Me 4-CF₃207-210 127 H Et H 2-Me 4-CF₃ >240 128 H Me H 2-Me 4-CF₃ 236-237 129 Hi-Pr H 4-F 4-OCF₃ 208-209 130 H CH(CH₃)CH₂OCH₃ H 4-F 4-OCF₃ 151-152 131H CH(CH₃)CH₂OCH₃ H 2-Me 4-CF₃ 188-190 132 CH₂CO₂Me i-Pr H H 4-CF₃ oil133 CH₂CO₂Me i-Pr H H 4-OCF₃ oil 134 Me Et H 2-Me 4-CF₃ oil 135 Me Et H2-Me 4-OCF₃ oil 136 Me Et H 2-Me 2-Me-4-SCF₂H 132-136 137 HCH(CH₃)CH₂OCH₃ H 2-Me-4-Br 4-CF₃ 197-199 138 H CH(CH₃)CH₂OCH₃ H2-Me-4-Br 4-OCF₃ 188-190 139 H i-Pr H 3-Cl 4-CF₃ 201-202 140 H t-Bu H3-Cl 4-CF₃ 159-161 141 H i-Pr H 3-Cl 4-OCF₃ 190-192 142 H t-Bu H 3-Cl4-OCF₃ 150-152 143 H iPr H 2-Br-4-Me 4-CF₃ >230 144 H t-Bu H 2-Br-4-Me4-CF₃ 213-215 145 H CH(CH₃)CH₂OCH₃ H 5-F 4-CF₃ 145-147 146 H

H 2-Me 4-CF₃ >230 147 H i-Pr H 2-Me 2-F-4-CF₃ 224-226 148 H i-Pr H 2-Me2-CF₃-4-F 223-225 149 H t-Bu H 4-F 4-OCF₃ 180-187 150 H CH(CH₃)CH₂OCH₃ H2-Me 2-Me-4-CF₃ 194-197 151 H Me H 2-Me 2-Me-4-CF₃ >230 152 H Et H 2-Me2-Me-4-CF₃ 243-245 153 H

H 2-Me 2-Me-4-CF₃ >230 154 H i-Pr H 3-NO₂ 4-CF₃ 244-246 155 H i-Pr H3-NO₂ 4-OCF₃ 239-240 156 H t-Bu H 3-NO₂ 4-OCF₃ 180-184 157 HCH(CH₃)CH₂OCH₃ H 3-NO₂ 4-OCF₃ 172-175 158 H t-Bu H 3-NO₂ 4-CF₃ 194-196159 H CH(CH₃)CH₂OCH₃ H 3-NO₂ 4-CF₃ 178-179 160 H i-Pr H 2-Cl 4-CF₃ >230161 H CH(CH₃)CH₂OCH₃ H 2-Cl 4-CF₃ 182-185 162 H t-Bu H 5-Cl 2-Me-4-CF₃203-205 163 H CH(CH₃)CH₂OCH₃ H 5-Cl 2-Me-4-CF₃ 154-155 164 H i-Pr H 2-Me2,4-(CF₃)₂ >230 165 H i-Pr H 2-Me 3,4-OCF₂O— 199-200 166 H CH₂CN H 2-Me4-CF₃ 218-223 167 H CH(CH₃)Ph H 2-Me 4-CF₃ 225-228 168 H CH(CH₃)Ph H2-Me 4-OCF₃ 208-210 169 H t-Bu H 2-Cl 4-CF₃ 191-193 170 H i-Pr Me 2-Cl4-CF₃ 136-140 171 H i-Pr H 2-Me 4-SO₂CH₃ >250 172 H i-Pr H 5-Cl 4-CF₃217-218 173 H t-Bu H 5-Cl 4-CF₃ 231-235 174 H CH(CH₃)CH₂OCH₃ H 5-Cl4-CF₃ 175-177 175 H i-Pr H 4-I 4-CF₃ >230 176 H t-Bu H 4-I 4-CF₃ 215-219177 H CH(CH₃)CH₂OCH₃ H 4-I 4-CF₃ 173-178 178 H i-Pr H 4-I 4-OCF₃ >230179 H t-Bu H 4-I 4-OCF₃ 192-194 180 H CH(CH₃)CH₂OCH₃ H 4-I 4-OCF₃178-180 181 H CH₂(3-pyridinyl) H 2-Me 4-CF₃ 198-199 182 H CH₂CN H 2-Me2-Me-4-CF₃ >230 183 H CH(CH₃)CO₂CH₃ H 2-Me 4-CF₃ 223-225 184 H i-Pr H2-F 4-CF₃ 228-229 185 H i-Pr H 5-F 4-CF₃ 169-170 186 H i-Pr H 2-F2-Me-4-OCF₃ 206-208 187 H i-Pr H 5-F 2-Me-4-OCF₃ 125-126 188 H i-Pr H2-F 2-Me-4-CF₃ 234-235 189 H i-Pr H 5-F 2-Me-4-CF₃ 133-135 190 HCH₂(3-pyridinyl) H 2-Me 4-OCF₃ 201-202 191 H CH₂CH₂SCH₃ H 2-Me 4-CF₃187-188 192 H CH₂CH₂SCH₃ H 2-Me 2-Me-4-CF₃ 250-251 193 H CH₂CH₂SEt H2-Me 4-CF₃ 190-191 194 H CH₂CH₂SEt H 2-Me 2-Me-4-CF₃ 228-230 195 HCH(CH₃)CH═CH₂ H 2-Me 2-Me-4-CF₃ 211-214 196 H i-Pr H 2-Et 4-CF₃ 228-230197 H CH(CH₃)CH₂OCH₃ H 2-Et 4-CF₃ 176-177 198 H i-Pr H 2-Me3,4-OCF₂CF₂O— 218-220 199 H i-Pr H 2-Me 2-(CONMe₂-4,5-Cl₂ 229-230 200 Hi-Pr H 2-Me 2-(CO-1-piperidinyl)- 202-205 4,5-Cl₂ 201 H t-Bu H 2-Et4-CF₃ 187-191 202 H CH(CH₃)CH₂SCH₃ H 2-Et 2-Me-4-CF₃ 206-208 203 H i-PrH 2-Me 2-(CONMe₂)-4-Br 191-194 204 H i-Pr H 2-Me 2-(CONMe₂)-5-Br 190-194205 H CH(CH₃)CH₂SO₂CH₃ H 2-Me 2-Me-4-CF₃ 231-233 206 H c-Pr H 2-Me2-Me-4-CF₃ 258-261 207 H c-Pr H 2-Cl 2-Me-4-CF₃ >260 208 H i-Pr H 2-I2-Me-4-OCF₃ 241-242 209 H i-Pr H 2-I 2-Me-4-CF₃ 260-262 210 H i-Pr H2-Me 2-(CONMe₂)-4-F 164-170 211 H i-Pr H 2-Me 2-(CONMe₂)-5-F 167-171 212H i-Pr H 2-Me 2-(CO-1-piperidinyl)-4- 105-117 Br 213 H CH(CH₃)CH₂OH H2-Me 2-Me-4-CF₃ 179-180 214 H CH(CH₃)CH₂OH H 2-Cl 2-Me-4-CF₃ 183-185 215H i-Pr H 2-Cl 2-(CONMe₂)-4-Br 165-170 216 H i-Pr H 2-Cl 2-(CONMe₂)-5-Br179-181 217 H i-Pr H 2-Me 2-(3-CF₃-1-pyrazolyl)-4- 243-244 CF₃ 218 Hi-Pr H 2-Me 2-(1-(1,2,4-triazolyl))-4- 238-240 CF₃ 219 H i-Pr H 2-Me2-(3-Br-1-pyrazolyl)-4- >250 CF₃ 220 H i-Pr H 2-Me2-(3-CN-1-pyrazolyl)-4- >250 CF₃ 221 H i-Pr H 2-Me2-(4-CF₃-1-imidazolyl)- >250 4-CF₃ 222 H i-Pr H 2-Me2-(3-CH₃-1-pyrazolyl)- 248-250 4-CF₃ 223 H i-Pr H 2-Me2-(2-CH₃-1-imidazolyl)- 186-188 4-CF₃ 224 H i-Pr H 2-Me2-(3-CF3-1-(1,2,4- 254-256 triazolyl))-4-CF₃ 225 H i-Pr H 2-Me2-(1-pyrazolyl)-4-CF₃ 246-248 226 H i-Pr H 2-Me 2-(3-CO₂Et-5-Me-1-224-225 pyrazolyl)-4-CF₃ 227 H i-Pr H 2-Me 2-(1-imidazolyl)-4-CF₃240-241 228 H i-Pr H 2-Me 2-(3-CF₃-5-Me-1- 229-231 pyrazolyl)-4-CF₃ 229H i-Pr H 2-Me 2-(3,5-Me₂-1-pyrazolyl)- 214-218 4-CF₃ 230 H i-Pr H 2-Me2-(2,4-Me₂-1- 246-248 imdazolyl)-4-CF₃ 231 H i-Pr H 2-Me2-(4-Me-1-imidazolyl)- 223-225 4-CF₃ 232 H i-Pr H 2-Cl2-(3-CF₃-1-pyrazolyl)-4- >250 CF₃ 233 H i-Pr H 2-Cl2-(1-(1,2,4-triazolyl))-4- 252-254 CF₃ 234 H i-Pr H 2-Cl2-(3-Br-1-pyrazolyl)-4- >250 CF₃ 235 H i-Pr H 2-Cl 2-(3-CO₂Et-5-Me-1-220-221 pyrazolyl)-4-CF₃ 236 H i-Pr H 2-Cl 2-(4-CO₂Me-1- 255-257imidazolyl)-4-CF₃ 237 H i-Pr H 2-Cl 2-(3-CN-1-pyrazolyl)-4- >250 CF₃ 238H i-Pr H 2-Cl 2-(1-imidazolyl)-4-CF₃ 248-249 239 H i-Pr H 2-Me2-(4-CO₂Me-1- 219-222 imidazolyl)-4-CF₃ 240 H i-Pr H 2-Me2-(2-thienyl)-4-CF₃ 241-243 241 H i-Pr H 2-Me 2-(3-thienyl)-4-CF₃229-231 242 H i-Pr H 2-Me 2-(2-furanyl)-4-CF₃ 246-247 243 H i-Pr H 2-Me2-(3-t-Bu-1-pyrazolyl)-4- 247-249 CF₃ 244 H i-Pr H 2-Me2-(3-s-Bu-1-pyrazolyl)- 224-225 4-CF₃ 245 H i-Pr H 2-Me2-(3-c-Pr-1-pyrazolyl)-4- 220-221 CF₃ 246 H i-Pr H 2-Me2-(3-Me-5-isoxazolyl)-4- 233-234 CF₃ 247 H i-Pr H 2-Me 2-

-4-CF₃ >250 248 H i-Pr H 2-Me 2-(CONMe₂)-4-CF₃ 188-192 249 H i-Pr H 2-Me2-(CONMe₂)-5-CF₃ 194-196 250 H i-Pr H 2-Me 2-(CO-1-pyrrolidinyl)-4-201-204 CF₃ 251 H i-Pr H 2-Me 2-(CO-1-pyrrolidinyl)-5- 221-223 CF₃ 252 Hi-Pr H 2-Me 2-OCH₃-4-CF₃ 188-189 253 H i-Pr H 2-Me2-(3-Cl-5-isoxazolyl)-4- 247-248 CF₃ 254 H i-Pr H 2-Me 2-Oi-Pr-4-CF₃158-159 255 H i-Pr H 2-Cl 2-(4-Me-1-pyrazolyl)-4- 252-253 CF₃ 256 H i-PrH 2-Me 2-(4-Me-1-pyrazolyl)-4- 226-227 CF₃ 257 H i-Pr H 2,5-Cl₂2-Me-4-CF₃ 235-237 258 H i-Pr H 2-Me 4-Ph 221-224 259 H i-Pr H 2-Me4-(4-OCH₃)Ph >230 260 H i-Pr H 2-Me 4-(2-Me)Ph 156-158 261 H i-Pr H 2-Me4-(3-CH₃)Ph 225-226 262 H i-Pr H 2-Me 4-(3-CF₃)Ph 214-215 263 H i-Pr H2-Me 4-(4-F)Ph >230 264 H —CH₂CH₂CH₂CH₂— 2-Cl 3-Cl 158-161 265 H

H 2-Me 4-OCF₃ >230 266 H i-Pr H 2-CF₃ 2-Me-4-Br >230 267 H t-Bu H 2-CF₃2-Me-4-Br 234-236 268 H i-Pr Me 2-CF₃ 2-Me-4-Br 154-158 269 HCH(CH₃)CH₂OCH₃ H 2-CF₃ 2-Me-4-Br 202-204 270 H s-Bu H 2-CF₃2-Me-4-Br >230 271 H s-pentyl H 2-CF₃ 2-Me-4-Br 215-217 272 H i-Pr H2-CH₃ 2-Me-4-CF₃ >230 273 H i-Pr Me 2-OCHF₂ 2-Me-4-Br 224-227 274 H i-PrH 2-CH₃ 2-(CONMe₂)-4-CF₃ 130-137 275 B is S H i-Pr H 2-Me 2-Me-4-CF₃193-195 276 H i-Pr H 2-Cl 2-(1-pyrazolyl)-4-CF₃ 249-250 277 B is S Hi-Pr H 2-Me 4-OCF₃ 169-171 278 B is S H i-Pr H 2-Me 4-CF₃Ph 204-206

[0371] INDEX TABLE B

R⁷(c) is H, except where indicated and B is O, except where indicatedCompound R² R³ (R⁴)_(n) R⁷(a) R⁷(b) m.p. ° C. B1 (Ex. 4) i-Pr H 2-Me CF₃CH₃ 247-248 B2 i-Pr H 2-Me OCH₂CF₃ H 188-191 B3 i-Pr H 2-Cl CF₃ CH₃234-236 B4 t-Bu H 2-Cl CF₃ CH₃ 243-245 B5 CH(CH₃)CH₂OCH₃ H 2-Cl CF₃ CH₃198-201 B6 CH(CH₃)CH═CH₂ H 2-Me CF₃ CH₃ 226-227 B7 i-Pr H 2-Cl OCH₂CF₃ H208-210 B8 t-Bu H 2-Cl OCH₂CF₃ H 174-175 B9 CH(CH₃)CH₂OCH₃ H 2-ClOCH₂CF₃ H 163-165 B10 i-Pr H 2-Me CF₃ H 208-211 B11 CH(CH₃)CH₂OCH₃ H2-Me CF₃ CH₃ 187-191 B12 s-Bu H 2-Me CF₃ CH₃ 215-218 B13 2-pentyl H 2-MeCF₃ CH₃ 213-215 B14 i-Pr H 2-Me Cl H 235-237 B15 i-Pr H 2-Me H Cl235-237 B16 i-Pr H 2-OCHF₂ CF₃ CH₃ 221-224 B17 i-Pr H 2-Me CF₂CF₃ CH₃208-209 B18 t-Bu H 2-Me CF₂CF₃ CH₃ 211-212 B19 CH(CH₃)CH₂OCH₃ H 2-MeCF₂CF₃ CH₃ 193-196 B20 t-Bu H 2-CF₃ CF₃ CH₃ >250 B21 t-Bu H 2-CF₃ CF₃CH₃ 218-222 B22 CH(CH₃)CH₂OCH₃ H 2-CF₃ CF₃ CH₃ 200-202 B23 i-Pr H 2-MeCF₃ Br 253-255 B24 CH(CH₃)CH₂SCH₃ H 2-Me CF₃ CH₃ 222-223 B25CH(CH₃)CH₂CN H 2-Me CF₃ CH₃ 230-232 B26 CH₂CH₂CN H 2-Me CF₃ CH₃ >260 B27c-Pr H 2-Me CF₃ CH₃ >260 B28 i-Pr H 2-Me CF₃ OCH₃ 181-183 B29 i-Pr H2-Me Cl CH₃ 246-247 B30 i-Pr H 2-Me CF₃ Ph >250 B31 i-Pr H 2-I CF₃ CH₃256-257 B32 i-Pr H 2-F CF₃ CH₃ 218-220 B33 i-Pr H 5-F CF₃ CH₃ 144-146B34 CH(CH₃)CH₂SO₂CH₃ H 2-Me CF₃ CH₃ 243-245 B35 CH(CH₃)CH₂OH H 2-Me CF₃CH₃ 222-223 B36 CH(CH₃)CH₂CO₂CH₃ H 2-Me CF₃ CH₃ 204-206 B37 i-Pr H 2-MeCF₃ CH₂OCH₃ 241-242 B38 i-Pr H 2-Me CF₃ CH₂CH₃ 229-231 B39 i-Pr H 2-MeCH₃ Cl 236-237 B40 i-Pr H 2-Me CH₃ 2-pyridinyl 278-281 B41 t-Bu H 2-MeCF₃ CH₃ 234-236 B42 i-Pr H 2-Me CF₃ n-Pr 224-226 B43 i-Pr Me 2-Me CF₃CH₃ 202-205 B44 i-Pr H 2-Me c-Pr CH₃ 226-229 B45 i-Pr H 2-Me c-Pr CH₃,HCl salt >230 B46 i-Pr H 2-Me CF₃ Cl 248-254 B47 i-Pr H 2-Me CF₃ i-Pr235-237 B48 i-Pr H 2-Me CF₃ 1-(1,2,4-triazolyl) >260 B49 i-Pr H 2-Br CF₃CH₃ 247-248 B50 i-Pr H 2-Me OCH₂CF₃ CH₃ 150-160 B51 i-Pr H 2-Me CF₃2-phenoxy 231-232 B52 i-Pr H 2-Me CF₃ 1-morpholinyl >250 B53 i-Pr H 2-MeCF₃ 1-(3-CF₃-imidazolyl) 247-250 B54 i-Pr H 2-Me CF₃1-(3-Br-pyrazolyl) >260 B55 i-Pr H 2-Me CF₃ 1-(3-CF₃-pyrazolyl) >260 B56i-Pr H 2-Me CF₃ 1-((3-CF₃)-1,2,4-triazolyl) >260 B57 i-Pr H 2-Me CF₃1-((3-CN)-1,2,4-triazolyl) >260 B58 i-Pr H 2-Me i-Bu Cl 185-190 B59 i-PrH 2-Me CF₃ 2-MePh 200-203 B60 i-Pr H 2-Me i-Pr CH₃ 186-190 B61 i-Pr H2-Me Ph Cl 229-234 B62 i-Pr H 2-Me CF₃ SCH₂CH(CH₃)₂ 230-231 B63 i-Pr H2-Me CF₂CF₃ CH₂CH₃ 209-211 B64 i-Pr H 2-Me CF₃ 1-pyrazolyl >250 B65 i-PrH 2-Me CF₂CF₃ H >250 B66 i-Pr H 2-Me CF₂CF₃ i-Pr 209-212 B67 i-Pr H2-Me, 4-Br CF₃ CH₃ >250 B68 i-Pr H 2-Me OCH₂CF₃ n-Pr 165-169 B69 i-Pr H2-Me Cl n-Pr 200-205 B70 i-Pr H 2-Me Cl Et 200-205 B71 i-Pr H 2-Me CF₃CN 214-215 B72 i-Pr H 2,5-Cl₂ CF₃ CH₃ >240 B73 i-Pr H 2-Me H H, R⁷(c) isSPh 223-225 B74 B is S, i-Pr H 2-Me CF₃ CH₃ 201-203 B75 B is S, i-Pr H2-Me CF₃ Et 173-175 B76 B is S, i-Pr H 2-Me CF₂CF₃ CH₃ 156-158 B77 i-PrH 2-Me H 1-((3-CF₃)-pyrazolyl) 224-225 B78 i-Pr H 2-Me CF₃ 2-ClPh223-225

[0372] INDEX TABLE C

B is O, except where indicated Compound R² R³ (R⁴)_(n) R⁷(a) R⁷(b) m.p.° C. C1 (Ex. 5) i-Pr H 2-Me CF₃ CH₃ 252-253 C2 i-Pr H 2-Cl CF₃ CH₃260-262 C3 i-Pr H 2-Me CF₃ OCH₃ 195-196 C4 i-Pr H 2-Me CF₃ N(CH₃)₂270-272 C5 i-Pr H 2-Me CF₃ Et 246-248 C6 i-Pr H 2-Me CF₃ Ph 175-177 C7i-Pr H 2-Me i-Pr Et 179-182 C8 i-Pr H 2-Me c-Pr Et 202-204 C9 i-Pr H2-Me i-Pr CH₃ 206-209 C10 i-Pr H 2-Me c-Pr CH₃ 222-225 C11 i-Pr H 2-Mec-Pr Ph 236-239 C12 i-Pr H 2-Me CF₃ SCH₃ 244-247 C13 i-Pr H 2-Me CF₃1-pyrrolidinyl 272-273 C14 i-Pr H 2-Me CF₃ OCH₂C(Cl)═CH₂ 142-144 C15 EtH 2-Me CF₃ 2-MePh 253-256 C16 i-Pr H 2-Me CF₃ 2-MePh 244-246 C17 t-Bu H2-Me CF₃ 2-MePh 251-253 C18 Et H 2-Cl CF₃ 2-MePh 242-243 C19 i-Pr H 2-ClCF₃ 2-MePh 237-240 C20 t-Bu H 2-Cl CF₃ 2-MePh 253-255 C21 Et H 2-Me CF₃2-ClPh 251-252 C22 i-Pr H 2-Me CF₃ 2-ClPh 246-248 C23 t-Bu H 2-Me CF₃2-ClPh 238-239 C24 Et H 2-Cl CF₃ 2-ClPh 248-249 C25 i-Pr H 2-Cl CF₃2-ClPh 254-255 C26 t-Bu H 2-Cl CF₃ 2-ClPh 240-242 C27 Et H 2-Me CF₃ c-Pr236-238 C28 i-Pr H 2-Me CF₃ c-Pr 240-241 C29 t-Bu H 2-Me CF₃ c-Pr246-248 C30 Et H 2-Cl CF₃ c-Pr 240-242 C31 i-Pr H 2-Cl CF₃ c-Pr 232-235C32 t-Bu H 2-Cl CF₃ c-Pr 266-268 C33 Et H 2-Me CF₃ i-Pr 230-231 C34 i-PrH 2-Me CF₃ i-Pr 211-214 C35 t-Bu H 2-Me CF₃ i-Pr 210-213 C36 Et H 2-ClCF₃ i-Pr 247-249 C37 i-Pr H 2-Cl CF₃ i-Pr 236-239 C38 t-Bu H 2-Cl CF₃i-Pr 235-238 C39 Et H 2-Me CF₂CF₃ 2-MePh 247 C40 i-Pr H 2-Me CF₂CF₃2-MePh 218-220 C41 t-Bu H 2-Me CF₂CF₃ 2-MePh 224-226 C42 Et H 2-ClCF₂CF₃ 2-MePh 241-243 C43 i-Pr H 2-Cl CF₂CF₃ 2-MePh 232-234 C44 t-Bu H2-Cl CF₂CF₃ 2-MePh 237-239 C45 Et H 2-Me CF₂CF₃ 2-ClPh 255-257 C46 i-PrH 2-Me CF₂CF₃ 2-ClPh 224 C47 t-Bu H 2-Me CF₂CF₃ 2-ClPh 215 C48 Et H 2-ClCF₂CF₃ 2-ClPh 248-250 C49 i-Pr H 2-Cl CF₂CF₃ 2-ClPh 222-224 C50 t-Bu H2-Cl CF₂CF₃ 2-ClPh 242 C51 Et H 2-Me CF₂CF₃ Ph 246-248 C52 i-Pr H 2-MeCF₂CF₃ Ph 220 C53 t-Bu H 2-Me CF₂CF₃ Ph 242 C54 Et H 2-Cl CF₂CF₃ Ph238-240 C55 i-Pr H 2-Cl CF₂CF₃ Ph 260 C56 t-Bu H 2-Cl CF₂CF₃ Ph 231-232C57 i-Pr H 2-Me CF₂CF₃ CH₃ 208 C58 t-Bu H 2-Me CF₂CF₃ CH₃ 242-244 C59 EtH 2-Cl CF₂CF₃ CH₃ 210-212 C60 i-Pr H 2-Cl CF₂CF₃ CH₃ 195 C61 t-Bu H 2-ClCF₂CF₃ CH₃ 246-248 C62 Et H 2-Me CF₂CF₃ c-Pr 224-225 C63 i-Pr H 2-MeCF₂CF₃ c-Pr 232-234 C64 Et H 2-Cl CF₂CF₃ c-Pr 216-218 C65 i-Pr H 2-ClCF₂CF₃ c-Pr 218-220 C66 t-Bu H 2-Cl CF₂CF₃ c-Pr 210-212 C67 Et H 2-MeCF₂CF₃ i-Pr 218-220 C68 i-Pr H 2-Me CF₂CF₃ i-Pr 196-198 C69 t-Bu H 2-MeCF₂CF₃ i-Pr 212-214 C70 Et H 2-Cl CF₂CF₃ i-Pr 216-220 C71 i-Pr H 2-ClCF₂CF₃ i-Pr 215-218 C72 t-Bu H 2-Cl CF₂CF₃ i-Pr 240-244 C73 i-Pr H 2-MeCF₂CF₃ Et 210-212 C74 Et H 2-Me CF₂CF₃ Et 230-232 C75 Et H 2-Cl CF₂CF₃Et 210-213 C76 i-Pr H 2-Cl CF₂CF₃ Et 203-204 C77 t-Bu H 2-Cl CF₂CF₃ Et230-232 C78 Et H 2-Me CF₂CF₃ CH₃ 238-240 C79 B is S i-Pr H 2-Me CF₃ Et190-193 C80 i-Pr H 2-Me CF₃ 2-CF₃Ph 255-258

[0373] INDEX TABLE D

R⁷ (c) is H, except where indicated and B is O, except where indicatedCompound R² R³ (R⁴)_(n) R⁷(a) R⁷(b) m.p. ° C. D1 i-Pr H 2-Me CF₃ CH₃200-204 D2 (Ex. 2) i-Pr H 2-Me CF₃ Et 123-126 D3 i-Pr H 2-Cl CF₃ CH₃233-235 D4 t-Bu H 2-Me CF₃ Et 215-218 D5 i-Pr H 2-Me CH₃ Ph 238-239 D6i-Pr H 2-Me CH₃ CH₃ 206-208 D7 i-Pr H 2-Me CH₃ CH₂CF₃ 246-248 D8 i-Pr H2-Cl Et CF₃ 235-237 D9 i-Pr H 2-Me CH₃ CH₃, R⁷ (c) is Cl 205-207 D10i-Pr H 2-Me CH₃ 4-CF₃Ph 256-258 D11 i-Pr H 2-Me CH₃ 2-CF₃Ph 204-206 D12t-Bu H 2-Me CH₃ Ph 236-238 D13 i-Pr H 2-F CH₃ Ph 227-229 D14 i-Pr H 5-FCH₃ Ph 209-211 D15 i-Pr H 2-Cl CH₃ Ph 233-234 D16 i-Pr H H CH₃ Ph215-217 D17 i-Pr H 2-NO₂ CH₃ Ph 236-237 D18 i-Pr H 2-Cl CF₃ Ph 240-242D19 (Ex. 6) i-Pr H 2-Me CF₃ Ph 260-262 D20 i-Pr H 2-I CH₃ Ph 250-251 D21i-Pr H 2-I CH₃ 2-CF₃Ph 251-253 D22 H H 2-Me CH₃ Ph 253-255 D23 Et Et2-Me CH₃ Ph 182-184 D24 t-Bu H 2-Cl CF₃ Ph 232-234 D25 i-Pr H 2-I CF₃ Ph271-273 D26 t-Bu H 2-I CF₃ Ph 249-250 D27 i-Pr H 2-Me CH₃ t-Bu 210-211D28 i-Pr H 2-Br CF₃ Ph 257-259 D29 i-Pr H 2-Br CH₃ Ph 246-247 D30 i-Pr H2-Me CF₃ 2-pyridinyl 237-238 D31 i-Pr H 2,5-Cl₂ CF₃ Ph >250 D32 B is S,i-Pr H 2-Me CF₃ Ph 169-172 D33 i-Pr H 2-Me CF₃ 2-ClPh 208-209 D34 i-Pr H2-Cl CF₃ 2-ClPh 234-235 D35 i-Pr H 2-Me CF₃ 4-ClPh 289-290 D36 i-Pr H2-Cl CF₃ 4-ClPh 276-278 D37 i-Pr H 2-Cl CF₃ 2-pyridinyl 239-240 D38 i-PrH 2-Me CF₃ 2-pyrimidinyl 205-208 D39 i-Pr H 2-Me CF₃ 2-(3-CH₃-pyridinyl)183-187 D40 i-Pr H 2-Me CF₂CF₃ Ph 231-232 D41 i-Pr H 2-Cl CF₂CF₃ Ph206-207 D42 t-Bu H 2-Cl CF₂CF₃ Ph 212-213 D43 i-Pr H 2-Br CF₂CF₃ Ph219-222 D44 i-Pr H 2-Me CF₃ 3-ClPh 278-280 D45 i-Pr H 2-Cl CF₃ 3-ClPh272-273 D46 i-Pr H 2-Me CF₃ 2-FPh 217-218 D47 i-Pr H 2-Cl CF₃ 2-FPh220-221 D48 i-Pr H 2-Me CF₃ 4-FPh 269-270 D49 i-Pr H 2-Cl CF₃ 4-FPh279-280 D50 i-Pr H 2-I c-Pr CH₃ 222-224 D51 i-Pr H 5-I c-Pr CH₃ 215-217D52 i-Pr H 2-CF₃ CF₃ Ph 247-249 D53 i-Pr H 2-Cl CF₃ i-Pr 255-258 D54i-Pr H 2-Me CF₃ 3-FPh 277-278 D55 i-Pr H 2-Cl CF₃ 3-FPh 256-257 D56 i-PrH 2-Me CF₃ 2-CF₃Ph 215-216 D57 i-Pr H 2-Cl CF₃ 2-CF₃Ph 230-231 D58 i-PrH 2-Me CF₃ 2-BrPh 207-208 D59 i-Pr H 2-Cl CF₃ 2-BrPh 239-240 D60 i-Pr H2-OCH₃ CF₃ Ph 215-216 D61 i-Pr H 5-Cl CF₃ 2-(3-CH₃-pyridinyl) 224-225D62 i-Pr H 5-Me CF₃ 2-(3-Cl-pyridinyl) 179-181 D63 s-Bu H 2-Cl CF₃Ph >240 D64 c-Pr H 2-Cl CF₃ Ph >240 D65 Et H 2-Cl CF₃ Ph >240 D66 t-Bu H2-CF₃ CF₃ Ph 230-233 D67 Et H 2-CF₃ CF₃ Ph 246-249 D68 CH(CH₃)CH₂SCH₃ H2-CF₃ CF₃ Ph 215-217 D69 CH(CH₃)CH₂OCH₃ H 2-CF₃ CF₃ Ph 220-223 D70 i-PrH 5-Cl CF₃ 2-(3-Cl-pyridinyl) 230-233 D71 i-Pr H 5-Me CF₃ 2-thiazolyl201-203 D72 i-Pr H 5-Me CF₃ 2-pyrazinyl 252-253 D73 i-Pr H 5-Me CF₃4-pyridinyl 224-228 D74 i-Pr H 2-Me CF₃ i-Pr 236-243 D75 i-Pr H 2-Me CF₃2-CH₃Ph 211-212 D76 i-Pr H 2-Cl CF₃ 2-CH₃Ph 232-234 D77 i-Pr H 2-Br CF₃2-ClPh 247-248 D78 t-Bu H 2-Me CF₃ 2-ClPh 216-217 D79 (Ex. 7) i-Pr H2-Me CF₃ 2-(3-CF₃-pyridinyl) 227-230 D80 CH₂CH₂Cl H 2-Cl CF₃ Ph 237-242D81 CH₂CH₂CH₂Cl H 2-Cl CF₃ Ph 233-239 D82 CH(CH₃)CO₂CH₃ H 2-Cl CF₃ Ph221-222 D83 S-CH(i-Pr)CO₂CH₃ H 2-Cl CF₃ Ph 212-213 D84 i-Pr H 2-Me CF₃2,6-Cl₂—Ph 267-268 D85 i-Pr H 2-Cl CF₃ 2,6-Cl₂—Ph 286-287 D86 i-Pr H2-Me Br Ph 253-255 D87 i-Pr H 2-Cl Br Ph 247-248 D88 i-Pr H 2-Me CF₃i-Bu 205-210 D89 i-Pr H 2-Me CF₃ CH₂Ph 235-237 D90 i-Pr H 2-Me CF₃2-(3-OCH₃-pyridinyl) 221-222 D91 i-Pr H 2-Me CF₃ 3-pyridinyl 260-261 D92i-Pr H 2-Me CF₃ 4-quinolinyl >260 D93 i-Pr H 2-Me CN 2-(3-Cl-pyridinyl)203-204 D94 i-Pr H 2-Me CF₃ 2,4-F₂—Ph 245-246 D95 i-Pr H 2-Cl CF₃2,4-F₂—Ph 252-253 D96 i-Pr H 2-Me CF₃ 2-Et—Ph 207-209 D97 i-Pr H 2-ClCF₃ 2-Et—Ph 221-222 D98 i-Pr H H CF₃ 2-ClPh 206-207 D99 t-Bu H H CF₃2-ClPh 197-198 D100 CH(CH₃)CH₂OCH₃ H H CF₃ 2-ClPh 145-148 D101CH(CH₃)CH₂SCH₃ H H CF₃ 2-ClPh 158-160 D102 CH(CH₃)CH₂SCH₃ H 2-Cl CF₃ Ph184-186 D103 CH(CH₃)CH₂OCH₃ H 2-Cl CF₃ Ph 217-218 D104 n-Pr H 2-Cl CF₃Ph 247-248 D105 i-Bu H 2-Cl CF₃ Ph 244-245 D106 CH₃ H 2-Cl CF₃ Ph >250D107 i-Pr Me 2-Cl CF₃ Ph 193-194 D108 CH₂C≡CH H 2-Cl CF₃ Ph >250 D109CH₂CH═CH₂ H 2-Cl CF₃ Ph 248-249 D110 CH₂(2-furanyl) H 2-Cl CF₃ Ph246-247 D111 i-Pr H 2-Me Ph 2-ClPh 133-136 D112 i-Pr H 2-Cl Ph 2-ClPh220-221 D113 1-Pr H 2-Me CF₃ 4-(3,5-Cl₂-pyridinyl) 239-242 D114 i-Pr H2-Cl CF₃ 4-(3,5-Cl₂-pyridinyl) 229-231 D115 CH(CH₃)CH₂SCH₃ H 2-Me CF₃2-ClPh 194-195 D116 CH(CH₃)CH₂OCH₃ H 2-Me CF₃ 2-ClPh 181-183 D117 s-Bu H2-Me CF₃ 2-ClPh 199-200 D118 c-Pr H 2-Me CF₃ 2-ClPh 234-235 D119 n-Pr H2-Me CF₃ 2-ClPh 222-223 D120 i-Bu H 2-Me CF₃ 2-ClPh 235-237 D121 Me H2-Me CF₃ 2-ClPh 242-243 D122 i-Pr Me 2-Me CF₃ 2-ClPh 90-93 D123 CH₂C≡CHH 2-Me CF₃ 2-ClPh 215-216 D124 Et H 2-Me CF₃ 2-ClPh 228-229 D125CH₂CH═CH₂ H 2-Me CF₃ 2-ClPh 227-228 D126 CH₂(2-furanyl) H 2-Me CF₃2-ClPh 218-219 D127 CH(CH₃)CH₂SCH₃ H 2-Me CF₃ Ph 179-180 D128CH(CH₃)CH₂OCH₃ H 2-Me CF₃ Ph 219-220 D129 s-Bu H 2-Me CF₃ Ph 244-245D130 c-Pr H 2-Me CF₃ Ph >250 D131 n-Pr H 2-Me CF₃ Ph 238-239 D132 i-Bu H2-Me CF₃ Ph 237-238 D133 Me H 2-Me CF₃ Ph 263-265 D134 i-Pr Me 2-Me CF₃Ph 178-179 D135 CH₂C≡CH H 2-Me CF₃ Ph 253-254 D136 Et H 2-Me CF₃ Ph244-245 D137 CH₂CH═CH₂ H 2-Me CF₃ Ph 240-241 D138 CH₂(2-furanyl) H 2-MeCF₃ Ph 245-246 D139 i-Pr H 2-OCHF₂ CF₃ 2-ClPh 200-201 D140 i-Pr H 2-OCH₃CF₃ 2-ClPh 206-207 D141 i-Pr H 2-I CF₃ 2-ClPh 253-256 D142 i-Pr H 2-MeBr 2-ClPh 147-150 D143 i-Pr H 2-Cl Br 2-ClPh 246-247 D144 i-Pr H 2-MeCF₃ 2-OCH₃Ph 218-219 D145 i-Pr H 2-Cl CF₃ 2-OCH₃Ph 243-244 D146 i-Pr H2-Me CF₃ 1-isoquinolinyl 252-253 D147 CH(CH₃)CH₂SCH₃ H 2-Cl CF₃ 2-ClPh217-218 D148 CH(CH₃)CH₂OCH₃ H 2-Cl CF₃ 2-ClPh 207-208 D149 s-Bu H 2-ClCF₃ 2-ClPh 216-217 D150 c-Pr H 2-Cl CF₃ 2-ClPh 261-262 D151 n-Pr H 2-ClCF₃ 2-ClPh 231-232 D152 i-Bu H 2-Cl CF₃ 2-ClPh 255-256 D153 Me H 2-ClCF₃ 2-ClPh 233-235 D154 i-Pr Me 2-Cl CF₃ 2-ClPh 127-128 D155 CH₂C≡CH H2-Cl CF₃ 2-ClPh 226-227 D156 Et H 2-Cl CF₃ 2-ClPh 244-246 D157 CH₂CH═CH₂H 2-Cl CF₃ 2-ClPh 235-236 D158 CH₂(2-furanyl) H 2-Cl CF₃ 2-ClPh 207-208D159 i-Pr H C≡CSi(CH₃)₃ CF₃ 2-ClPh 256-258 D160 i-Pr H C≡CH CF₃ 2-ClPh228-230 D161 i-Pr H 2-Cl C≡CH 2-ClPh 219-222 D162 i-Pr H 2-Me H H, R⁷(c)is CH₃ 220-223 D163 i-Pr H 2-Me CH₃ Ph, R⁷(c) is Cl 209-210 D164 B is S i-Pr H 2-Cl CF₃ Ph 169-174 D165 i-Pr H 2-Me CF₃ 2,6-F₂Ph 223-225 D166i-Pr H 2-Me CF₃ 2-Cl-6-FPh 203-206 D167 i-Pr H 2-Cl CF₃ 2-Cl-6-FPh218-221 D168 i-Pr H 2-Me-4-Br CF₃ 2-FPh 232-233 D169 t-Bu H 2-Cl CF₃2-(3-Cl-pyridinyl) 250-251 D170

H 2-Cl CF₃ 2-(3-Cl-pyridinyl) >250 D171 Et Et 2-Cl CF₃ 2-ClPh 243-247D172 Me Me 2-Cl CF₃ 2-ClPh 234-235 D173 Et Et 2-Me CF₃ 2-ClPh 237-238D174 Me Me 2-Me CF₃ 2-ClPh 225-226 D175 CH₂CH₂N(Me)₂ H 2-Me CF₃ 2-ClPh188-190 D176 i-Pr H 2-Cl CF₃ 2-pyrazinyl 242-243 D177 t-Bu H 2-Me-4-BrCF₃ 2-ClPh >260 D178 CH(CH₃)CH₂OCH₃ H 2-Me CF₃ 2-(3-Cl-pyridinyl)176-177 D179 CH(CH₃)CH₂SCH₃ H 2-Me CF₃ 2-(3-Cl-pyridinyl) 196-197 D180CH(CH₃)CH₂OCH₃ H 2-Cl CF₃ 2-(3-Cl-pyridinyl) 197-198 D181 CH(CH₃)CH₂SCH₃H 2-Cl CF₃ 2-(3-Cl-pyridinyl) 202-203 D182 i-Pr H 2-Me CF₃ 2-IPh 221-222D183 i-Pr H 2-Cl CF₃ 2-IPh 238-240 D184 i-Pr H 2-Me CF₃ 2-(C≡CH)—Ph215-217 D185 i-Pr H 2-Cl CF₃ 2-(C≡CH)—Ph 244-246 D186 t-Bu H 2-Cl CF₃2-(3-Cl-pyridinyl) 250-251 D187

H 2-Cl CF₃ 2-(3-Cl-pyridinyl) >250 D188 i-Pr H 2-Me CF₃ 2-Cl-4-FPh203-205 D189 i-Pr H 2-Cl CF₃ 2-Cl-4-FPh 218-219 D190 Me Me 2-Me CF₃2-ClPh 225-226 D191 Et Et 2-Me CF₃ 2-ClPh 243-247 D192 i-Pr H 2-Me CF₃2,6-Me₂Ph 259-260 D193 i-Pr H 2-Cl CF₃ 2,6-Me₂Ph 268-269 D194 i-Pr H2-Me CF₃ 2,6-Cl₂-4-CNPh * D195 i-Pr H 2-Me CF₃ 2-CNPh 225-235 D196 i-PrH 2-Me CF₃ 2-(OCF₃)Ph 214-215 D197 i-Pr H 2-Cl CF₃ 2-(OCF₃)Ph 223-224D198 i-Pr H 2-Me CF₃ 2-Br-4-FPh 202-203 D199 i-Pr H 2-Cl CF₃ 2-Br-4-FPh222-223 D200 i-Pr H 2-Me CF₃ 2-(3-Me-pyrazinyl) 205-207 D201 Me H 2-ClCF₃ 2-(3-Cl-pyridinyl) 215-220 D202 CH₂C≡CH H 2-Cl CF₃2-(3-Cl-pyridinyl) 197-198 D203 Me H 2-Me CF₃ 2-(3-Cl-pyridinyl) 193-196D204 Et H 2-Me CF₃ 2-(3-Cl-pyridinyl) 204-206 D205 CH₂C≡CH H 2-Me CF₃2-(3-Cl-pyridinyl) 177-178 D206 i-Pr H 2-Me CF₃ 4-(8-Cl-quinolinyl) >250D207 i-Pr H 2-Me CF₃ 4-(2-Me-quinolinyl) >250 D208 i-Pr H 2-Cl CF₃4-(2-Me-quinolinyl) >250 D209 i-Pr H 2-Me CF₃ 4-(7-Cl-quinolinyl) >250D210 i-Pr H 2,4-Br₂ CF₃ 2-ClPh 233-234 D211 i-Pr H 2-Br Br 2-ClPh255-258 D212 Me H 2-Me Br 2-ClPh 236-237 D213 t-Bu H 2-Cl Br 2-ClPh260-261 D214 Et H 2-Me Br 2-ClPh 254-255 D215 t-Bu H 2-Me Br 2-ClPh259-260 D216 c-Bu H 2-Cl CN 2-(3-Cl-pyridinyl) 177-180 D217 i-Pr H 2-MeCF₃ 2-(3-Cl-pyridinyl) 237-239 D218 i-Pr H 2-Me CF₃4-(6-Cl-quinolinyl) >250 D219 Me Me 2-Me CF₃ 4-(6-Cl-quinolinyl) >250D220 O-i-Pr H 2-Cl CF₃ 2-ClPh 218-219 D221 i-Pr H 2-Cl CN2-(3-Cl-pyridinyl) 195-200 D222 t-Bu H 2-Cl CN 2-(3-Cl-pyridinyl) >250D223 Et H 2-Cl CN 2-(3-Cl-pyridinyl) 200-205 D224 i-Pr H 2-Cl CF₃2-(3-Me-pyrazinyl) 225-230 D225 t-Bu H 2-Cl CF₃ 2-(3-Me-pyrazinyl)235-240 D226 Et H 2-Cl CF₃ 2-(3-Me-pyrazinyl) 210-220 D227 i-Pr H 2-MeCF₃ 3-(2-Cl-pyridinyl) * D228 i-Pr H 2-Cl CF₃ 2,3-Cl₂Ph 217-219 D229t-Bu H 2-Cl CF₃ 2,3-Cl₂Ph 254-256 D230 i-Pr H 2-Me CF₃ 2,3-Cl₂Ph 208-209D231 t-Bu H 2-Me CF₃ 2,3-Cl₂Ph 232-233 D232 t-Bu H 2-Me-4-Br Br 2-ClPh239-241 D233 Me H 2-Me-4-Br Br 2-ClPh 150-152 D234 Et H 2-Me-4-Br Br2-ClPh 223-225 D235 i-Pr H 2-Me-4-Br Br 2-ClPh 197-198 D236 Me H 2-MeCF₃ 2-FPh 245-247 D237 CH₂C≡CH H 2-Me CF₃ 2-FPh 222-227 D238 O-i-Pr H2-Cl CN 2-(3-Cl-pyridinyl) 205-206 D239 O-i-Pr H 2-Me CN2-(3-Cl-pyridinyl) 210-211 D240 Me Me 2-Cl CF₃ 2-ClPh 234-236 D241CH₂C≡CH H 2-Me-4-Br Br 2-ClPh 187-188

[0374] INDEX TABLE E

Com- pound R² R³ (R⁴)_(n) R⁷(a) R⁷(b) R⁷(c) m.p. ° C. E1 i-Pr H 2-Me CH₃CH₃ H 143-145 E2 i-Pr H 2-Me CH₃ CH₂CF₃ H 198-199 E3 i-Pr H 2-Me CH₃ CH₃Cl 188-190 E4 i-Pr H 2-Me CH₃ 4-CF₃—Ph H 198-199 E5 i-Pr H 2-Me CH₃2-CF₃—Ph H 211-213 E6 i-Pr H 2-Me CH₃ t-Bu H 125-127 E7 i-Pr H 2-Me CF₃CH₂Ph H 130-135 E8 i-Pr H 2-Me H Ph CH₃ 249-250 E9 i-Pr H 2-Me H CH₃ Ph268-270 E10 i-Pr H 2-Cl H Ph CH₃ 260-261 E11 i-Pr H 2-Me H CH₂CF₃ Ph213-215 E12 i-Pr H 2-Cl H CH₂CF₃ Ph 208-209 E13 i-Pr H 2-Me H CHF₂ Ph *E14 i-Pr H 2-Me CF₃ 2-(3-Cl-pyridinyl) H 249-250

[0375] INDEX TABLE F

Com- pound R² R³ (R⁴)_(n) R⁷(a) R⁷(b) R⁷(c) m.p. ° C. F1 i-Pr H 2-MeCH₂CF₃ CH₃ H 254-255 F2 i-Pr H 2-Me CH₂CF₃ H CH₃ 200-205 F3 i-Pr H 2-MeCH₂(3-CF₃)Ph H CH₃ 212-215 F4 i-Pr H 2-Cl CH₂CF₃ H CH₃ 215-217 F5 i-Pr H2-Me Ph H CF₃ 223-224 F6 i-Pr H 2-Cl Ph H CF₃ 206-208 F7 i-Pr H 2-MeCH₂CF₃ H Ph 156-158 F8 i-Pr H 2-Cl CH₂CF₃ H Ph 162-164

[0376] INDEX TABLE G

Compound Q R² R³ (R⁴)_(n) R⁷(a) R⁷(b) m.p. ° C. G1 S i-Pr H 2-Me4-OCF₃Ph CH₃ 233-234 G2 S i-Pr H 2-Me OCH₂CF₂CF₃ CH₃ 170-173 G3 S i-Pr H2-Me Cl CH₃ 164-167 G4 S i-Pr H 2-Me CH₃ Ph 216-219 G5 S i-Pr H 2-MeC(CH₃)₂OH CH₃ * G6 S i-Pr H 2-Me i-Pr CH₃ 180-181 G7 S i-Pr H 2-Me i-PrPh 182-183 G8 O i-Pr H 2-Me i-Pr CH₃ 163-164

[0377] INDEX TABLE H

Compound Q R² R³ (R⁴)_(n) R⁷(a) R⁷(b) R⁷(c) m.p. ° C. H1 S i-Pr H 2-Me HH H 192-195 H2 S CH(CH₃)CH₂OCH₃ H 2-Me H H H 120-123 H3 S t-Bu H 2-Me HH H 120-123 H4 NMe i-Pr H 2-Me Me H H 193-195 H5 NPh i-Pr H 2-Me H Me H188-192 H6 NPh i-Pr H 2-Me Br H H 176-179 H7 NPh i-Pr H 2-Me Br H Br215-216 H8 NPh i-Pr H 2-Me H H Br 150-154 H9 NPh i-Pr H 2-Me CF₃ H H182-184 H10 N(2-ClPh) i-Pr H 2-Me Br H H 100-110 H11 N(2-FPh) i-Pr H2-Me Br H H 178-179 H12 N(2-FPh) t-Bu H 2-Me Br H H 186-188 H13N(2-ClPh) t-Bu H 2-Me Br H H 225-229

[0378] INDEX TABLE J

Compound R² R³ (R⁴)_(n) R⁷(a) R⁷(b) m.p. ° C. J1 i-Pr H 2-Me Me Me221-222 J2 i-Pr H H CF₃ Ph 279-281 J3 i-Pr H 2-Me CF₃ Ph 263-268 J4 i-PrH 2-Cl CF₃ 2-ClPh 235-238 J5 i-Pr H 2-Cl CF₃ Ph 245-246 J6 i-Pr H 2-MeCF₃ 2-ClPh 240-242 J7 i-Pr H 2-Cl CF₃ 2-F-4-ClPh 246-247 J8 i-Pr H 2-MeCF₃ 2-F-4-ClPh 266-268 J9 i-Pr H 2-Me CF₃ 2-pyridinyl 258-260

[0379] INDEX TABLE K

Compound R² R³ (R⁴)_(n) R⁷(a) R⁷(b) m.p. ° C. K1 i-Pr H 2-Me Br H177-180 K2 t-Bu H 2-Me Br H 188-194

[0380] INDEX TABLE L

Compound R² R³ (R⁴)_(n) R⁷(a) R⁷(b) m.p. ° C. L1 i-Pr H 2-Me Me Me203-205 L2 i-Pr H 2-Me Me 2,6-Cl₂Ph 218-223

[0381] INDEX TABLE M

Compound Q R² R³ (R⁴)_(n) R⁷(a) R⁷(b) R⁷(c) m.p. ° C. M1 S i-Pr H 2-MeCl Me H 203-205 M2 S i-Pr H 2-Cl Cl Me H 210-213 M3 NCHF₂ t-Bu H 2-Me HH Ph 165-166 M4 NH i-Pr H 2-Me CF₃ Ph H 118-120 M5 NMe i-Pr H 2-Me CF₃Ph H 110-112 M6 NCHF₂ i-Pr H 2-Me 2-FPh H H 143-144 M7 NCHF₂ t-Bu H 2-Me2-FPh H H 120-123 M8 NCH₂CF₃ i-Pr H 2-Me 2-FPh H H 235-237

[0382] INDEX TABLE N

Compound Het m.p. ° C. N1

169-171 N2

227-230 N3

243-246

[0383] INDEX TABLE P Compound m.p. ° C. P1

178-179

[0384] INDEX TABLE Q Compd. No. ¹H NMR Data (CDCl₃ solution unlessindicated otherwise)^(a) D194 (DMSO-d6) δ 1.03 (d, 6H), 2.18 (s, 3H),3.92 (m, 1H), 7.22-7.30 (m, 2H), 7.35 (m, 1H), 7.62 (dd, 1H), 7.81 (s,1H), 8.02 (d, 1H), 8.15 (dd, 1H), 8.55 (dd, 1H), 10.34 (s, 1H). D227(DMSO-d6) δ 1.01 (d, 6H), 2.16 (s, 3H), 3.92 (m, 1H), 7.27 (m, 2H), 7.35(m, 1H), 7.89 (s, 1H), 7.96 (m, 1H), 8.37 (s, 2H), 10.42 (s, 1H). G5 δ1.22 (d, 6H), 2.05 (s, 6H), 2.31 (s, 3H), 2.76 (s, 3H), 4.18 (m, 1H),5.94 (d, 1H), 7.20 (dd, 1H), 7.29 (d, 1H), 7.38 (d, 1H), 9.83 (br s,1H). E13 δ 1.12 (d, 6H), 2.32 (s, 1H), 4.14 (m 1H), 4.95 (d, 1H), 7.19(dd, 1H), 7.28 (t, 1H), 7.32 (m, 5H), 7.59 (dd, 2H), 7.92 (s, 1H), 9.51(br s, 1H).

BIOLOGICAL EXAMPLES OF THE INVENTION TEST

[0385] Application: Compounds are formulated in a 10% acetone, 90% waterand 300 ppm X-77 surfactant solution, unless otherwise indicated. Theformulated compounds are applied with a SUJ2 atomizer nozzle with ⅛ JJcustom body (Spraying Systems) positioned ½″ above the top of each testunit. There are 6 of these nozzles that make up the spray boom and thisis fixed in a belt sprayer. A rack (or carrier) of 6 different insecttest units is placed on the conveyor belt and stops so that each unit iscentered under a nozzle. Once the rack is centered, 1 mL of liquid issprayed into each test unit; the rack then continues down the belt tothe end of the sprayer to be off-loaded. All experimental compounds inthis screen are sprayed at 250 ppm and replicated three times.

[0386] Diamondback Moth (DBM)—Plutella Xylostella: The test unitconsists of a small self-contained unit with a 12-14 day old radishplant inside. These are pre-infested (using a core sampler) with 10-15neonate larvae on a piece of insect diet. Once 1 mL of formulatedcompound has been sprayed into each test unit, the test units areallowed to dry for 1 hour before a black, screened cap is placed on thetop of the cylinder. They are held for 6 days in a growth chamber at 25° C. and 70% relative humidity.

[0387] Plant feeding damage was visually assessed on a scale of 0-10where 0 is no feeding, 1 is 10% or less feeding, 2 is 20% or lessfeeding, 3 is 30% or less feeding through a maximum score of 10 where 10is 100% of foliage consumed. Of the compounds tested the followingprovided excellent levels of plant protection (ratings of 0-1, 10% orless feeding damage): 1, 2, 3, 4, 6, 7, 9, 10, 13, 14, 15, 19, 20, 24,27, 28, 29, 30, 31, 32, 33, 35, 37, 38, 39, 51, 52, 53, 60, 61, 62, 63,64, 65, 66, 68, 69, 72, 73, 74, 75, 76, 79, 80, 84, 86, 88, 89, 90, 92,96, 97, 98, 99, 100, 101, 102, 103, 107, 113, 124, 126, 127, 143, 144,146, 147, 148, 150, 151, 152, 153, 158, 159, 160, 161, 162, 163, 164,165, 166, 167, 169, 170, 171, 174, 183, 184, 185, 186, 187, 188, 189,190, 191, 193, 194, 195, 196, 198, 202, 203, 204, 205, 206, 207, 208,209, 210, 211, 212, 213, 214, 215, 216, 217, 218, 219, 220, 222, 223,225, 227, 228, 229, 230, 231, 232, 233, 235, 238, 239, 240, 244, 245,246, 248, 249, 250, 251, 252, 253, 256, 257, 275, 276, 277, 278, B2, B4,B5, B6, B7, B8, B9, B10, B11, B12, B13, B14, B15, B16, B17, B18,B19,B20, B21, B23, B24, B25, B28, B29, B30, B31, B32, B33, B35, B37, B38,B39, B40, B42, B43, B44, B45, B46, B47, B48, B49, B50, B53, B55, B57,B58, B59, B60, B61, B62, B63, B64, B66, B67, B68, B69, B70, B71, B72,B74, B75, B76, C1, C2, C3, C4, C5, C7, C8, C9, C10, C11, C12, C79, D2,D3, D4, D5, D6, D7, D8, D11, D12, D13, D14, D15, D16, D18, D19, D20,D23, D24, D25, D26, D27, D28, D29, D30, D32, D33, D34, D37, D38, D39,D40, D41, D42, D45, D46, D47, D48, D50, D51, D52, D53, D54, D55, D56,D57, D58, D59, D60, D61, D62, D63, D64, D65, D66, D67, D68, D69, D70,D71, D72, D73, D74, D75, D76, D77, D78, D79, D81, D83, D84, D85, D86,D87, D88, D89, D91, D92, D93, D94, D95, D96, D97, D111, D113, D114,D115, D116, D117, D118, D119, D120, D121, D122, D123, D124, D125, D126,D162, D164, E4, F2, F5, F6, F7, F8, G2, G3, G5, H1, H2, H3, H4, J3, J4,J6, M1, M3, N2 and P1.

What is claimed is:
 1. A method for controlling arthropods comprisingcontacting the arthropods or their environment with an arthropodicidallyeffective amount of a compound of Formula 1, its N-oxide oragriculturally suitable salts

wherein A and B are independently O or S; each J is independently aphenyl or naphthyl group substituted with 1 to 2 R⁵ and optionallysubstituted with 1 to 3 R⁶; or each J is independently a 5- or6-membered heteroaromatic ring or an aromatic 8-, 9- or 10-memberedfused heterobicyclic ring system wherein each ring or ring system isoptionally substituted with 1 to 4 R⁷; n is 1 to 4; R¹ is H; or C₁-C₆alkyl, C₂-C₆ alkenyl, C₂-C₆ alkynyl or C₃-C₆ cycloalkyl each optionallysubstituted with one or more substituents selected from the groupconsisting of halogen, CN, NO₂, hydroxy, C₁-C₄ alkoxy, C₁-C₄ alkylthio,C₁-C₄ alkylsulfinyl, C₁-C₄ alkylsulfonyl, C₂-C₄ alkoxycarbonyl, C₁-C₄alkylamino, C₂-C₈ dialkylamino and C₃-C₆ cycloalkylamino; or R¹ is C₂-C₆alkylcarbonyl, C₂-C₆ alkoxycarbonyl, C₂-C₆ alkylaminocarbonyl, C₃-C₈dialkylaminocarbonyl or C(═A)J; R² is H, C₁-C₆ alkyl, C₂-C₆ alkenyl,C₂-C₆ alkynyl, C₃-C₆ cycloalkyl, C₁-C₄ alkoxy, C₁-C₄ alkylamino, C₂-C₈dialkylamino, C₃-C₆ cycloalkylamino, C₂-C₆ alkoxycarbonyl or C₂-C₆alkylcarbonyl; R³ is H; G; C₁-C₆ alkyl, C₂-C₆ alkenyl, C₂-C₆ alkynyl,C₃-C₆ cycloalkyl, each optionally substituted with one or moresubstituents selected from the group consisting of halogen, G, CN, NO₂,hydroxy, C₁-C₄ alkoxy, C₁-C₄ haloalkoxy, C₁-C₄ alkylthio, C₁-C₄alkylsulfinyl, C₁-C₄ alkylsulfonyl, C₂-C₆ alkoxycarbonyl, C₂-C₆alcylcarbonyl, C₃-C₆ trialklsilyl, or a phenyl, phenoxy or 5- or6-membered heteroaromatic ring, each ring optionally substituted withone to three substituents independently selected from the groupconsisting of C₁-C₄ alkyl, C₂-C₄ alkenyl, C₂-C₄ alkynyl, C₃-C₆cycloalkyl, C₁-C₄ haloalkyl, C₂-C₄ haloalkenyl, C₂-C₄ haloalkynyl, C₃-C₆halocycloalkyl, halogen, CN, NO₂, C₁-C₄ alkoxy, C₁-C₄ haloalkoxy, C₁-C₄alkylthio, C₁-C₄ alkylsulfinyl, C₁-C₄ alkylsulfonyl, C₁-C₄ alkylamino,C₂-C₈ dialkylamino, C₃-C₆ cycloalkylamino, C₃-C₆ (alkyl)cycloalkylamino,C₂-C₄ alkylcarbonyl, C₂-C₆ alkoxycarbonyl, C₂-C₆ alkylaminocarbonyl,C₃-C₈ dialkylaminocarbonyl or C₃-C₆ trialkylsilyl; C₁-C₄ alkoxy; C₁-C₄alkylamino; C₂-C₈ dialkylamino; C₃-C₆ cycloalkylamino; C₂-C₆alkoxycarbonyl or C₂-C₆ alkylcarbonyl; or R² and R³ can be takentogether with the nitrogen to which they are attached to form a ringcontaining 2 to 6 atoms of carbon and optionally one additional atom ofnitrogen, sulfur or oxygen, said ring may be optionally substituted with1 to 4 substituents selected from the group consisting of C₁-C₂ alkyl,halogen, CN, NO₂ and C₁-C₂ alkoxy; G is a 5- or 6-membered nonaromaticcarbocyclic or heterocyclic ring, optionally including one or two ringmembers selected from the group consisting of C(═O), SO or S(O)₂ andoptionally substituted with 1 to 4 substituents selected from the groupconsisting of C₁-C₂ alkyl, halogen, CN, NO₂ and C₁-C₂ alkoxy; each R⁴ isindependently H, C₁-C₆ alkyl, C₂-C₆ alkenyl, C₂-C₆ alkynyl, C₃-C₆cycloalkyl, C₁-C₆ haloalkyl, C₂-C₆ haloalkenyl, C₂-C₆ haloalkynyl, C₃-C₆halocycloalkyl, halogen, CN, NO₂, hydroxy, C₁-C₄ alkoxy, C₁-C₄haloalkoxy, C₁-C₄ alkylthio, C₁-C₄ alkylsulfonyl, C₁-C₄ alkylsulfonyl,C₁-C₄ haloalkylthio, C₁-C₄ haloalkylsulfinyl, C₁-C₄ haloalkylsulfonyl,C₁-C₄ alkylamino, C₂-C₈ dialkylamino, C₃-C₆ cycloalkylamino, or C₃-C₆trialkylsilyl; or each R⁴ is independently phenyl, benzyl or phenoxy,each optionally substituted with C₁-C₄ alkyl, C₂-C₄ alkenyl, C₂-C₄alkynyl, C₃-C₆ cycloalkyl, C₁-C₄ haloalkyl, C₂-C₄ haloalkenyl, C₂-C₄haloalkynyl, C₃-C₆ halocycloalkyl, halogen, CN, NO₂, C₁-C₄ alkoxy, C₁-C₄haloalkoxy, C₁-C₄ alkylthio, C₁-C₄ alkylsulfinyl, C₁-C₄ alkylsulfonyl,C₁-C₄ alkylamino, C₂-C₈ dialkylamino, C₃-C₆ cycloalkylamino, C₃-C₆(alkyl)cycloalkylamino, C₂-C₄ alkylcarbonyl, C₂-C₆ alkoxycarbonyl, C₂-C₆alkylaminocarbonyl, C₃-C₈ dialkylaminocarbonyl or C₃-C₆ trialkylsilyl;each R⁵ is independently C₁-C₆ alkyl, C₂-C₆ alkenyl, C₂-C₆ alkynyl,C₃-C₆ cycloalkyl, C₁-C₆ haloalkyl, C₂-C₆ haloalkenyl, C₂-C₆ haloalkynyl,C₃-C₆ halocycloalkyl, halogen, CN, CO₂H, CONH₂, NO₂, hydroxy, C₁-C₆alkoxy, C₁-C₆ haloalkoxy, C₁-C₆ alkylthio, C₁-C₆ alkylsulfinyl, C₁-C₆alkylsulfonyl, C₁-C₆ haloalkylthio, C₁-C₆ haloalkylsulfinyl, C_(l)-C₆haloalkylsulfonyl, C₁-C₆ alkylamino, C₂-C₁₂ dialkylamino, or C₃-C₆cycloalkylamino, C₂-C₆ alkylcarbonyl, C₂-C₆ alkoxycarbonyl, C₂-C₆alkylaminocarbonyl, C₃-C₈ dialkylaminocarbonyl, C₃-C₆ trialkylsilyl; or(R⁵)₂ when attached to adjacent carbon atoms can be taken together as—OCF₂O—, —CF₂CF₂O—, or —OCF₂CF₂O—; each R⁶ is independently H, halogen,C₁-C₆ alkyl, C₂-C₆ alkenyl, C₂-C₆ alkynyl, C₃-C₆ cycloalkyl, C₁-C₄alkoxy or C₂-C₄ alkoxycarbonyl; or each R⁶ is independently a phenyl,benzyl, phenoxy, 5- or 6-membered heteroaromatic ring or an aromatic 8-,9- or 10-membered fused heterobicyclic ring system, each ring optionallysubstituted with one to three substituents independently selected fromthe group consisting of C₁-C₄ alkyl, C₂-C₄ alkenyl, C₂-C₄ alkynyl, C₃-C₆cycloalkyl, C₁-C₄ haloalkyl, C₂-C₄ haloalkenyl, C₂-C₄ haloalkynyl, C₃-C₆halocycloalkyl, halogen, CN, NO₂, C₁-C₄ alkoxy, C₁-C₄ haloalkoxy, C₁-C₄alkylthio, C₁-C₄ alkylsulfinyl, C₁-C₄ alkylsulfonyl, C₁-C₄ alkylamino,C₂-C₈ dialkylamino, C₃-C₆ cycloalkylamino, C₃-C₆ (alkyl)cycloalkylamino,C₂-C₄ alkylcarbonyl, C₂-C₆ alkoxycarbonyl, C₂-C₆ alkylaminocarbonyl,C₃-C₈ dialkylaminocarbonyl or C₃-C₆ trialkylsilyl; each R⁷ isindependently H, C₁-C₆ alkyl, C₂-C₆ alkenyl, C₂-C₆ alkynyl, C₃-C₆cycloalkyl, C₁-C₆ haloalkyl, C₂-C₆ haloalkenyl, C₂-C₆ haloalkynyl, C₃-C₆halocycloalkyl, halogen, CN, CO₂H, CONH₂, NO₂, hydroxy, C₁-C₄ alkoxy,C₁-C₄ haloalkoxy, C₁-C₄ alkylthio, C₁-C₄ alkylsulfinyl, C₁-C₄alkylsulfonyl, C₁-C₄ haloalkylthio, C₁-C₄ haloalkylsulfinyl, C₁-C₄haloalkylsulfonyl, C₁-C₄ alkylamino, C₂-C₈ dialkylamino, C₃-C₆cycloalkylamino, C₂-C₆ alkylcarbonyl, C₂-C₆ alkoxycarbonyl, C₂-C₆alkylaminocarbonyl, C₃-C₈ dialkylaminocarbonyl, C₃-C₆ trialkylsilyl; oreach R⁷ is independently a phenyl, benzyl, benzoyl, phenoxy, 5- or6-membered heteroaromatic ring or an aromatic 8-, 9- or 10-memberedfused heterobicyclic ring system, each ring optionally substituted withone to three substituents independently selected from the groupconsisting of C₁-C₄ alkyl, C₂-C₄ alkenyl, C₂-C₄ alkynyl, C₃-C₆cycloalkyl, C₁-C₄ haloalkyl, C₂-C₄ haloalkenyl, C₂-C₄ haloalkynyl, C₃-C₆halocycloalkyl, halogen, CN, NO₂, C₁-C₄ alkoxy, C₁-C₄ haloalkoxy, C₁-C₄alkylthio, C₁-C₄ alkylsulfonyl, C₁-C₄ alkylsulfonyl, C₁-C₄ alkylamino,C₂-C₈ dialkylamino, C₃-C₆ cycloalkylamino, C₃-C₆ (alkyl)cycloalkylamino,C₂-C₄ alkylcarbonyl, C₂-C₆ alkoxycarbonyl, C₂-C₆ alkylaminocarbonyl,C₃-C₈ dialkylaminocarbonyl or C₃-C₆ trialkylsilyl; provided that (1)when A and B are both O, R² is H or C₁-C₃ alkyl, R³ is H or C₁-C₃ alkyland R⁴ is H, halogen, C₁-C₆ alkyl, phenyl, hydroxy or C₁-C₆ alkoxy, thenone R⁵ is other than halogen, C₁-C₆ alkyl, hydroxy or C₁-C₆ alkoxy; or(2) J is other than an optionally substituted 1,2,3-thiadiazole.
 2. Themethod of claim 1 wherein J is a phenyl group substituted with 1 to 2 R⁵and optionally substituted with 1 to 3 R⁶.
 3. The method of claim 2wherein A and B are both O; n is 1 to 2; R¹ is H, C₁-C₄ alkyl, C₂-C₄alkenyl, C₂-C₄ alkynyl, C₃-C₆ cycloalkyl, C₂-C₆ alkylcarbonyl or C₂-C₆alkoxycarbonyl; R² is H, C₁-C₄ alkyl, C₂-C₄ alkenyl, C₂-C₄ alkynyl,C₃-C₆ cycloalkyl, C₂-C₆ alkylcarbonyl or C₂-C₆ alkoxycarbonyl; R³ isC₁-C₆ alkyl, C₂-C₆ alkenyl, C₂-C₆ alkynyl or C₃-C₆ cycloalkyl eachoptionally substituted with one or more substituents selected from thegroup consisting of halogen, CN, C₁-C₂ alkoxy, C₁-C₂ alkylthio, C₁-C₂alkylsulfinyl and C₁-C₂ alkylsulfonyl; one of the R⁴ groups is attachedto the phenyl ring at the 2-position or 5-position, and said R⁴ is C₁-C₄alkyl, C₁-C₄ haloalkyl, halogen, CN, NO₂, C₁-C₄ alkoxy, C₁-C₄haloalkoxy, C₁-C₄ alkylthio, C₁-C₄ alkylsulfinyl, C₁-C₄ alkylsulfonyl,C₁-C₄ haloalkylthio, C₁-C₄ haloalkylsulfinyl, C₁-C₄ haloalkylsulfonyl;each R⁵ is independently C₁-C₄ haloalkyl, CN, NO₂, C₁-C₄ haloalkoxy,C₁-C₄ alkylthio, C₁-C₄ alkylsulfinyl, C₁-C₄ alkylsulfonyl, C₁-C₄haloalkylthio, C₁-C₄ haloallylsulfinyl, C₁-C₄ haloalkylsulfonyl or C₂-C₄alkoxycarbonyl; or (R⁵)₂ when attached to adjacent carbon atoms can betaken together as —OCF₂O—, —CF₂CF₂O— or —OCF₂CF₂O—; and each R⁶ isindependently H, halogen, C₁-C₄ alkyl, C₁-C₂ alkoxy or C₂-C₄alkoxycarbonyl, or each R⁶ is independently a phenyl or a 5- or6-membered heteroaromatic ring, each ring optionally substituted withC₁-C₄ alkyl, C₂-C₄ alkenyl, C₂-C₄ alkynyl, C₃-C₆ cycloalkyl, C₁-C₄haloalkyl, C₂-C₄ haloalkenyl, C₂-C₄ haloalknyl, C₃-C₆ halocycloalkyl,halogen, CN, NO₂, C₁-C₄ alkoxy, C₁-C₄ haloalkoxy, C₁-C₄ alkylthio, C₁-C₄alkylsulfinyl, C₁-C₄ alkylsulfonyl, C₁-C₄ alkylamino, C₂-C₈dialkylamino, C₃-C₆ cycloalkylamino, C₃-C₆ (alkyl)cycloalkylamino, C₂-C₄alkylcarbonyl, C₂-C₆ alkoxycarbonyl, C₂-C₆ alkylaminocarbonyl, C₃-C₈dialkylaminocarbonyl or C₃-C₆ trialkylsilyl.
 4. The method of claim 3wherein R¹ and R² are both H; R³ is C₁-C₄ alkyl optionally substitutedwith halogen, CN, OCH₃, S(O)_(p)CH₃; each R⁴ is independently H, CH₃,CF₃, OCF₃, OCHF₂, S(O)_(p)CF₃, S(O)_(p)CHF₂, CN or halogen; each R⁵ isindependently CF₃, OCF₃, OCHF₂, S(O)_(p)CF₃, S(O)_(p)CHF₂, OCH₂CF₃,OCF₂CHF₂, S(O)_(p)CH₂CF₃ or S(O)_(p)CF₂CHF₂; each R⁶ is independently H,halogen or methyl; or phenyl, pyrazole, imidazole; triazole, pyridine orpyrimidine, each ring optionally substituted with C₁-C₄ alkyl, C₁-C₄haloalkyl, halogen or CN; and p is 0, 1 or
 2. 5. The method of claim 4wherein R³ is i-propyl or t-butyl.
 6. The method of claim 1 wherein J isa 5- or 6-membered heteroaromatic ring optionally substituted with 1 to4 R⁷.
 7. The method of claim 6 wherein J is a 5- or 6-memberedheteroaromatic ring selected from the group consisting of J-1, J-2, J-3,J-4 and J-5, each J optionally substituted with 1 to 3 R⁷

Q is O, S or NR⁷; and W, X, Y and Z are independently N or CR⁷, providedthat in J-4 and J-5 at least one of W, X, Y or Z is N.
 8. The method ofclaim 6 or 7 wherein A and B are O; n is 1 to 2; R¹ is H, C₁-C₄ alkyl,C₂-C₄ alkenyl, C₂-C₄ alkynyl, C₂-C₆ alkylcarbonyl or C₂-C₆alkoxycarbonyl; R² is H, C₁-C₄ alkyl, C₂-C₄ alkenyl, C₂-C₄ alkynyl,C₃-C₆ cycloalkyl, C₂-₆ alkylcarbonyl or C₂-C₆ alkoxycarbonyl; R³ is H;or C₁-C₆ alkyl, C₂-C₆ alkenyl, C₂-C₆ alkynyl or C₃-C₆ cycloalkyl eachoptionally substituted with one or more substituents selected from thegroup consisting of halogen, CN, C₁-C₂ alkoxy, C₁-C₂ alkylthio, C₁-C₂alkylsulfinyl and C₁-C₂ alkylsulfonyl; one of the R⁴ groups is attachedto the phenyl ring at the 2-position, and said R⁴ is C₁-C₄ alkyl, C₁-C₄haloalkyl, halogen, CN, NO₂, C₁-C₄ alkoxy, C₁-C₄ haloalkoxy, C₁-C₄alkylthio, C₁-C₄ alkylsulfinyl, C₁-C₄ alkylsulfonyl, C₁-C₄haloalkylthio, C₁-C₄ haloalkylsulfinyl or C₁-C₄ haloalkylsulfonyl; andeach R⁷ is independently H, C₁-C₄ alkyl, C₁-C₄ haloalkyl, halogen, CN,NO₂, C₁-C₄ haloalkoxy, C₁-C₄ alkylthio, C₁-C₄ alkylsulfinyl, C₁-C₄alkylsulfonyl, C₁-C₄ haloalkylthio, C₁-C₄ haloalkylsulfinyl, C₁-C₄haloalkylsulfonyl or C₂-C₄ alkoxycarbonyl; or a phenyl or a 5- or6-membered heteroaromatic ring, each ring optionally substituted withC₁-C₄ alkyl, C₂-C₄ alkenyl, C₂-C₄ alkynyl, C₃-C₆ cycloalkyl, C₁-C₄haloalkyl, C₂-C₄ haloalkenyl, C₂-C₄ haloalkynyl, C₃-C₆ halocycloalkyl,halogen, CN, NO₂, C₁-C₄ alkoxy, C₁-C₄ haloalkoxy, C₁-C₄ alkylthio, C₁-C₄alkylsulfinyl, C₁-C₄ alkylsulfonyl, C₁-C₄ alkylamino, C₂-C₈dialkylamino, C₃-C₆ cycloalkylamino, C₃-C₆ (alkyl)cycloalkylamino, C₂-C₄alkylcarbonyl, C₂-C₆ alkoxycarbonyl, C₂-C₆ alkylaminocarbonyl, C₃-C₈dialkylaminocarbonyl or C₃-C₆ trialkylsilyl.
 9. The method of claim 8wherein J is selected from the group consisting of pyridine, pyrimidine,pyrazole, imidazole, triazole, thiophene, thiazole and oxazole, furan,isothiazole and isoxazole, each optionally substituted with 1 to 3 R⁷.10. The method of claim 9 wherein J is selected from the groupconsisting of pyridine, pyrimidine, pyrazole, thiophene and thiazole,each optionally substituted with 1 to 3 R⁷; R¹ and R² are both H; R³ isC₁-C₄ alkyl optionally substituted with halogen, CN, OCH₃, S(O)_(p)CH₃;each R⁴ is independently H, CH₃, CF₃, OCF₃, OCHF₂, S(O)_(p)CF₃,S(O)_(p)CHF₂, CN or halogen; each R⁷ is independently H, halogen, CH₃,CF₃, OCHF₂, S(O)_(p)CF₃, S(O)_(p)CHF₂, OCH₂CF₃, OCF₂CHF₂,S(O)_(p)CH₂CF₃, S(O)_(p)CF₂CHF₂; or phenyl, pyrazole, imidazole,triazole, pyridine or pyrimidine, each ring optionally substituted withC₁-C₄alkyl, C₁-C₄ haloalkyl, C₁-C₄ alkoxy, C₁-C₄ haloalkoxy, C₁-C₄alkylthio, C₁-C₄ alkylsulfinyl, C₁-C₄ alkylsulfonyl, halogen or CN; andp is 0, 1 or
 2. 11. The method of claim 10 wherein J is a pyridineoptionally substituted with 1 to 3 R⁷.
 12. The method of claim 11wherein one R⁷ is a phenyl optionally substituted with C₁-C₄ alkyl,C₁-C₄ haloalkyl, halogen or CN.
 13. The method of claim 11 wherein oneR⁷ is a pyrazole, imidazole, triazole, pyridine or pyrimidine, each ringoptionally substituted with C₁-C₄ alkyl, C₁-C₄ haloalkyl, halogen or CN.14. The method of claim 10 wherein J is a pyrimidine optionallysubstituted with 1 to 3 R⁷.
 15. The method of claim 14 wherein one R⁷ isa phenyl optionally substituted with C₁-C₄ alkyl, C₁-C₄ haloalkyl,halogen or CN.
 16. The method of claim 14 wherein one R⁷ is a pyrazole,imidazole, triazole, pyridine or pyrimidine, each ring optionallysubstituted with C₁-C₄ alkyl, C₁-C₄ haloalkyl, halogen or CN.
 17. Themethod of claim 10 wherein J is a pyrazole optionally substituted with 1to 3 R⁷.
 18. The method of claim 17 wherein one R⁷ is a phenyloptionally substituted with C₁-C₄ alkyl, C₁-C₄ haloalkyl, halogen or CN.19. The method of claim 17 wherein one R⁷ is a pyrazole, imidazole,triazole, pyridine or pyrimidine, each ring optionally substituted withC₁-C₄ alkyl, C₁-C₄ haloalkyl, halogen or CN.
 20. The method of claim 19wherein R⁷ is a pyridine optionally substituted with C₁-C₄ alkyl, C₁-C₄haloalkyl, halogen or CN.
 21. The method of claim 1 comprising acompound of Formula 1 selected from the group consisting of:3-methyl-N-(1-methylethyl)-2-[[4-(trifluoromethyl)benzoyl]amino]-benzamide,2-methyl-N-[2-methyl-6-[[(1-methylethyl)amino]carbonyl]phenyl]-4-(trifluoromethyl)benzamide,2-methyl-N-[2-methyl-6-[[(1-methylethyl)amino]carbonyl]phenyl]-6-(trifluoromethyl)-3-pyridinecarboxamide,1-ethyl-N-[2-methyl-6-[[(1-methylethyl)amino]carbonyl]phenyl]-3-(trifluoromethyl)-1H-pyrazole-5-carboxamide,1-(2-fluorophenyl)-N-[2-methyl-6-[[(1-methylethyl)amino)carbonyl]phenyl]-3-(trifluoromethyl)-1H-pyrazole-5-carboxamide,1-(3-chloro-2-pyridinyl)-N-[2-methyl-6-[[(1-methylethyl)amino]carbonyl]phenyl]3-(trifluoromethyl)-1H-pyrazole-5-carboxamide,N-[2-chloro-6-[[(1-methylethyl)amino]carbonyl]phenyl]-1-(3-chloro-2-pyridinyl)-3-(trifluoromethyl)-1H-pyrazole-5-carboxamide,3-bromo-1-(2-chlorophenyl)-N-[2-methyl-6-[[(1-methylethyl)amino]carbonyl]phenyl]-1H-pyrazole-5-carboxamide,and3-bromo-N-[2-chloro-6-[[(1-methylethyl)amino]carbonyl]phenyl]-1-(2-chlorophenyl)-1H-pyrazole-5-carboxamide.22. A compound of Formula 1, its N-oxides and agriculturally suitablesalts

wherein A and B are independently O or S; optionally substituted with 1to 3 R⁶; or each J is independently a 5- or 6-membered heteroaromaticring or an aromatic 8-, 9- or 10-membered fused heterobicyclic ringsystem wherein each ring or ring system is optionally substituted with 1to 4 R⁷; n is 1 to 4; R¹ is H; or C₁-C₆ alkyl, C₂-C₆ alkenyl, C₂-C₆alkynyl or C₃-C₆ cycloalkyl each optionally substituted with one or moresubstituents selected from the group consisting of halogen, CN, NO₂,hydroxy, C₁-C₄ alkoxy, C₁-C₄ alkylthio, C₁-C₄ alkylsulfinyl, C₁-C₄alkylsulfonyl, C₂-C₄ alkoxycarbonyl, C₁-C₄ alkylamino, C₂-C₈dialkylamino and C₃-C₆ cycloalkylamino; or R¹ is C₂-C₆ alkylcarbonyl,C₂-C₆ alkoxycarbonyl, C₂-C₆ alkylaminocarbonyl, C₃-C₈dialkylaminocarbonyl or C(═A)J; R² is H, C₁-C₆ alkyl, C₂-C₆ alkenyl,C₂-C₆ alkynyl, C₃-C₆ cycloalkyl, C₁-C₄ alkoxy, C₁-C₄ alkylamino, C₂-C₈dialkylamino, C₃-C₆ cycloalkylamino, C₂-C₆ alkoxycarbonyl or C₂-C₆alkylcarbonyl; R³ is H; C₁-C₆ alkyl, C₂-C₆ alkenyl, C₂-C₆ alkynyl, C₃-C₆cycloalkyl, each optionally substituted with one or more substituentsselected from the group consisting of halogen, CN, NO₂, hydroxy, C₁-C₄alkoxy, C₁-C₄ haloalkoxy, C₁-C₄ alkylthio, C₁-C₄ alkylsulfinyl, C₁-C₄alkylsulfonyl, C₂-C₆ akoxycarbonyl, C₂-C₆ alkylcarbonyl, C₃-C₆trialkylsilyl, or a phenoxy ring optionally substituted with one tothree substituents independently selected from the group consisting ofC₁-C₄ alkyl, C₂-C₄ alkenyl, C₂-C₄ alkynyl, C₃-C₆ cycloalkyl, C₁-C₄haloalkyl, C₂-C₄ haloalkenyl, C₂-C₄ haloalkynyl, C₃-C₆ halocycloalkyl,halogen, CN, NO₂, C₁-C₄ alkoxy, C₁-C₄ haloalkoxy, C₁-C₄ alkylthio, C₁-C₄alkylsulfinyl, C₁-C₄ alkylsulfonyl, C₁-C₄ alkylamino, C₂-C₈dialkylamino, C₃-C₆ cycloalkylamino, C₃-C₆ (alkyl)cycloalkylamino, C₂-C₄alkylcarbonyl, C₂-C₆ alkoxycarbonyl, C₂-C₆ alkylaminocarbonyl, C₃-C₈dialkylaminocarbonyl or C₃-C₆ trialkylsilyl; C₁-C₄ alkoxy; C₁-C₄alkylamino; C₂-C₈ dialkylamino; C₃-C₆ cycloalkylamino; C₂-C₆alkoxycarbonyl or C₂-C₆ alkylcarbonyl; or R² and R³ can be takentogether with the nitrogen to which they are attached to form a ringcontaining 2 to 6 atoms of carbon and optionally one additional atom ofnitrogen, sulfur or oxygen, said ring may be optionally substituted with1 to 4 substituents selected from the group consisting of C₁-C₂ alkyl,halogen, CN, NO₂ and C₁-C₂ alkoxy; each R⁴ is independently H, C₁-C₆alkyl, C₂-C₆ alkenyl, C₂-C₆ alkynyl, C₃-C₆ cycloalkyl, C₁-C₆ haloalkyl,C₂-C₆ haloalkenyl, C₂-C₆ haloalkynyl, C₃-C₆ halocycloalkyl, halogen, CN,NO₂, hydroxy, C₁-C₄ alkoxy, C₁-C₄ haloalkoxy, C₁-C₄ alkylthio, C₁-C₄alkylsulfinyl, C₁-C₄ alkylsulfonyl, C₁-C₄ haloalkylthio, C₁-C₄haloalkylsulfinyl, C₁-C₄ haloalkylsulfonyl, C₁-C₄ alkylamino, C₂-C₈dialkylamino, C₃-C₆ cycloalkylamino, or C₃-C₆ trialkylsilyl; or each R⁴is independently phenyl, benzyl or phenoxy, each optionally substitutedwith C₁-C₄ alkyl, C₂-C₄ alkenyl, C₂-C₄ alkynyl, C₃-C₆ cycloalkyl, C₁-C₄haloalkyl, C₂-C₄ haloalkenyl, C₂-C₄ haloalkynyl, C₃-C₆ halocycloalkyl,halogen, CN, NO₂, C₁-C₄ alkoxy, C₁-C₄ haloalkoxy, C₁-C₄ alkylthio, C₁-C₄alkylsulfinyl, C₁-C₄ alkylsulfonyl, C₁-C₄ alkylamino, C₂-C₈dialkylamino, C₃-C₆ cycloalkylamino, C₃-C₆ (allyl)cycloalkylamino, C₂-C₄alkylcarbonyl, C₂-C₆ alkoxycarbonyl, C₂-C₆ alkylaminocarbonyl, C₃-C₈dialkylaminocarbonyl or C₃-C₆ trialkylsilyl; each R⁵ is independentlyC₁-C₆ haloalkyl, C₂-C₆ haloalkenyl, C₂-C₆ haloalkynyl, C₃-C₆halocycloalkyl, C₁-C₄ haloalkoxy, C₁-C₄ alkylthio, C₁-C₄ alkylsulfinyl,C₁-C₄ alkylsulfonyl, C₁-C₄ haloalkylthio, C₁-C₄ haloalkylsulfinyl, C₁-C₄haloalkylsulfonyl, CN, NO₂, C₁-C₄ alkoxycarbonyl, C₁-C₄ alkylamino,C₂-C₈ dialkylamino, C₃-C₆ cycloalkylamino, C₂-C₆ alkylcarbonyl, C₂-C₆alkoxycarbonyl, C₂-C₆ alkylaminocarbonyl, or C₃-C₈ dialkylaminocarbonyl;or (R⁵)₂ attached to adjacent carbon atoms can be taken together as—OCF₂O—, —CF₂CF₂O—, or —OCF₂CF₂O—; each R⁶ is independently H, halogen,C₁-C₆ alkyl, C₂-C₆ alkenyl, C₂-C₆ alkynyl, C₃-C₆ cycloalkyl, C₁-C₄alkoxy or C₂-C₄ alkoxycarbonyl; or each R⁶ is independently a phenyl,benzyl, phenoxy, 5- or 6-membered heteroaromatic ring or an aromatic 8-,9- or 10-membered fused heterobicyclic ring system, each ring optionallysubstituted with one to three substituents independently selected fromthe group consisting of C₁-C₄ alkyl, C₂-C₄ alkenyl, C₂-C₄ alkynyl, C₃-C₆cycloalkyl, C₁-C₄ haloalkyl, C₂-C₄ haloalkenyl, C₂-C₄ haloalkynyl, C₃-C₆halocycloalkyl, halogen, CN, NO₂, C₁-C₄ alkoxy, C₁-C₄ haloalkoxy, C₁-C₄alkylthio, C₁-C₄ alkylsulfinyl, C₁-C₄ alkylsulfonyl, C₁-C₄ alkylamino,C₂-C₈ dialkylamino, C₃-C₆ cycloalkylamino, C₃-C₆ (alkyl)cycloalkylamino,C₂-C₄ alkylcarbonyl, C₂-C₆ alkoxycarbonyl, C₂-C₆ alkylaminocarbonyl,C₃-C₈ dialkylaminocarbonyl or C₃-C₆ trialkylsilyl; each R⁷ isindependently H, C₁-C₆ alkyl, C₂-C₆ alkenyl, C₂-C₆ alkynyl, C₃-C₆cycloalkyl, C₁-C₆ haloalkyl, C₂-C₆ haloalkenyl, C₂-C₆ haloalkynyl, C₃-C₆halocycloalkyl, halogen, CN, CO₂H, CONH₂, NO₂, hydroxy, C₁-C₄ alkoxy,C_(l)-C₄ haloalkoxy, C₁-C₄ alkylthio, C₁-C₄ alkylsulfinyl, C₁-C₄alkylsulfonyl, C₁-C₄ haloalkylthio, C₁-C₄ haloalkylsulfinyl, C₁-C₄haloalkylsulfonyl, C₁-C₄ alkylamino, C₂-C₈ dialkylamino, C₃-C₆cycloalkylamino, C₂-C₆ alkylcarbonyl, C₂-C₆ alkoxycarbonyl, C₂-C₆alkylaminocarbonyl, C₃-C₈ dialkylaminocarbonyl, C₃-C₆ trialkylsilyl; oreach R⁷ is independently a phenyl, benzyl, benzoyl, phenoxy or 5- or6-membered heteroaromatic ring 8-, 9- or 10-membered fusedheterobicyclic ring system, each ring optionally substituted with one tothree substituents independently selected from the group consisting ofC₁-C₄ alkyl, C₂-C₄ alkenyl, C₂-C₄ alkynyl, C₃-C₆ cycloalkyl, C₁-C₄haloalkyl C₂-C₄ haloalkenyl, C₂-C₄ haloalkynyl, C₃-C₆ halocycloalkyl,halogen, CN, NO₂, C₁-C₄ alkoxy, C₁-C₄ haloalkoxy, C₁-C₄ alkylthio, C₁-C₄alkylsulfinyl, C₁-C₄ alkylsulfonyl, C₁-C₄ alkylamino, C₂-C₈dialkylamino, C₃-C₆ cycloalkylamino, C₃-C₆ (allyl)cycloalkylamino, C₂-C₄alkylcarbonyl, C₂-C₆ alkoxycarbonyl, C₂-C₆ alkylaminocarbonyl, C₃-C₈dialkylaminocarbonyl or C₃-C₆ trialkylsilyl; provided that (i) at leastone R⁴ and at least one R⁷ are other than H; (ii) J is other than anoptionally substituted 1,2,3-thiadiazole; (iii) when J is an optionallysubstituted pyridine and R² is H, R³ is other than H or CH₃; (iv) when Jis an optionally substituted pyridine, then R⁷ cannot be CONH₂, C₂-C₆alkylaminocarbonyl or C₃-C₈ dialkylaminocarbonyl; (v) when J is anoptionally substituted pyrazole, tetrazole or pyrimidine, then R² and R³cannot both be hydrogen.
 23. The compound of claim 22 wherein J is aphenyl group substituted with 1 to 2 R⁵ and optionally substituted with1 to 3 R⁶.
 24. The compound of claim 25 wherein A and B are both O; n is1 to 2; R¹ is H, C₁-C₄ alkyl, C₂-C₄ alkenyl, C₂-C₄ alkynyl, C₃-C₆cycloalkyl, C₂-C₆ alkylcarbonyl or C₂-C₆ alkoxycarbonyl; R² is H, C₁-C₄alkyl, C₂-C₄ alkenyl, C₂-C₄ alkynyl, C₃-C₆ cycloalkyl, C₂-C₆alkylcarbonyl or C₂-C₆ alkoxycarbonyl; R³ is C₁-C₆ alkyl, C₂-C₆ alkenyl,C₂-C₆ alkynyl or C₃-C₆ cycloalkyl each optionally substituted with oneor more substituents selected from the group consisting of halogen, CN,C₁-C₂ alkoxy, C₁-C₂ alkylthio, C₁-C₂ alkylsulfinyl and C₁-C₂alkylsulfonyl; one of the R⁴ groups is attached to the phenyl ring atthe 2-position or 5-position, and said R⁴ is C₁-C₄ alkyl, C₁-C₄haloalkyl, halogen, CN, NO₂, C₁-C₄ alkoxy, C₁-C₄ haloalkoxy, C₁-C₄alkylthio, C₁-C₄ alkylsulfinyl, C₁-C₄ alkylsulfonyl, C₁-C₄haloalkylthio, C₁-C₄ haloalkylsulfinyl or C₁-C₄ haloalkylsulfonyl; eachR⁵ is independently C₁-C₄ haloalkyl, CN, NO₂, C₁-C₄ haloalkoxy, C₁-C₄alkylthio, C₁-C₄ alkylsulfinyl, C₁-C₄ alkylsulfonyl, C₁-C₄haloalkylthio, C₁-C₄ haloalkylsulfinyl, C₁-C₄ haloalkylsulfonyl or C₂-C₄alkoxycarbonyl; or (R⁵)₂ when attached to adjacent carbon atoms can betaken together as —OCF₂O—, —CF₂CF₂— or —OCF₂CF₂—; and each R⁶ isindependently H, halogen, C₁-C₄ alkyl, C₁-C₂ alkoxy or C₂-C₄alkoxycarbonyl, or each R⁶ is independently a phenyl or a 5- or6-membered heteroaromatic ring, each ring optionally substituted withC₁-C₄ alkyl, C₂-C₄ alkenyl, C₂-C₄ alkynyl, C₃-C₆ cycloalkyl, C₁-C₄haloalkyl, C₂-C₄ haloalkenyl, C₂-C₄ haloalkynyl, C₃-C₆ halocycloalkyl,halogen, CN, NO₂, C₁-C₄ alkoxy, C₁-C₄ haloalkoxy, C₁-C₄ alkylthio, C₁-C₄alkylsulfinyl, C₁-C₄ alkylsulfonyl, C₁-C₄ alkylamino, C₂-C₈dialkylamino, C₃-C₆ cycloalkylamino, C₃-C₆ (alkyl)cycloalkylamino, C₂-C₄alkylcarbonyl, C₂-C₆ alkoxycarbonyl, C₂-C₆ alkylaminocarbonyl, C₃-C₈dialkylaminocarbonyl or C₃-C₆ trialkylsilyl.
 25. The compound of claim26 wherein R¹ and R² arc both H; R³ is C₁-C₄ alkyl optionallysubstituted with halogen, CN, OCH₃, S(O)_(p)CH₃; each R⁴ isindependently H, CH₃, CF₃, OCF₃, OCHF₂, S(O)_(p)CF₃, S(O)_(p)CHF₂, CN orhalogen; each R⁵ is independently CF₃, OCF₃, OCHF₂, S(O)_(p)CF₃,S(O)_(p)CHF₂, OCH₂CF₃, OCF₂CHF₂, S(O)_(p)CH₂CF₃ or S(O)_(p)CF₂CHF₂; eachR⁶ is independently H, halogen or methyl; or phenyl, pyrazole,imidazole, triazole, pyridine or pyrimidine, each ring optionallysubstituted with C₁-C₄ alkyl, C₁-C₄ haloalkyl, halogen or CN; and p is0, 1 or
 2. 26. The compound of claim 25 wherein R³ is i-propyl ort-butyl.
 27. The compound of claim 26 wherein J is a 5- or 6-memberedheteroaromatic ring optionally substituted with 1 to 4 R⁷.
 28. Thecompound of claim 27 wherein J is a 5- or 6-membered heteroaromatic ringselected from the group consisting of J-1, J-2, J-3, J-4 and J-5, each Joptionally substituted with 1 to 3 R⁷

Q is O, S or NR⁷; and W, X, Y and Z are independently N or CR⁷, providedthat in J-4 and J-5 at least one of W, X, Y or Z is N.
 29. The compoundof claim 27 or claim 28 wherein A and B are O; n is 1 to 2; R¹ is H,C₁-C₄ alkyl, C₂-C₄ alkenyl, C₂-C₄ alkynyl, C₂-C₆ alkylcarbonyl or C₂-C₆alkoxycarbonyl; R² is H, C₁-C₄ alkyl, C₂-C₄ alkenyl, C₂-C₄ alkynyl,C₃-C₆ cycloalkyl, C₂-C₆ alkylcarbonyl or C₂-C₆ alkoxycarbonyl; R³ is H;or C₁-C₆ alkyl, C₂-C₆ alkenyl, C₂-C₆ alkynyl or C₃-C₆ cycloalkyl eachoptionally substituted with one or more substituents selected from thegroup consisting of halogen, CN, C₁-C₂ alkoxy, C₁-C₂ alkylthio, C₁-C₂alkylsulfinyl and C₁-C₂ alkylsulfonyl; one of the R⁴ groups is attachedto the phenyl ring at the 2-position, and said R⁴ is C₁-C₄ alkyl, C₁-C₄haloalkyl, halogen, CN, NO₂, C₁-C₄ alkoxy, C₁-C₄ haloalkoxy, C₁-C₄alkylthio, C₁-C₄ alkylsulfinyl, C₁-C₄ alkylsulfonyl, C₁-C₄haloalkylthio, C₁-C₄ haloalkylsulfinyl or C₁-C₄ haloalkylsulfonyl; andeach R⁷ is independently H, C₁-C₄ alkyl, C₁-C₄ haloalkyl, halogen, CN,NO₂, C₁-C₄ haloalkoxy, C₁-C₄ alkylthio, C₁-C₄ alkylsulfinyl, C₁-C₄alkylsulfonyl, C₁-C₄ haloalkylthio, C₁-C₄ haloalkylsulfinyl, C₁-C₄haloalkylsulfonyl or C₂-C₄ alkoxycarbonyl; or a phenyl or a 5- or6-membered heteroaromatic ring, each ring optionally substituted withC₁-C₄ alkyl, C₂-C₄ alkenyl, C₂-C₄ alkynyl, C₃-C₆ cycloalkyl, C₁-C₄haloalkyl, C₂-C₄ haloalkenyl, C₂-C₄ haloalkynyl, C₃-C₆ halocycloalkyl,halogen, CN, NO₂, C₁-C₄ alkoxy, C₁-C₄ haloalkoxy, C₁-C₄ alkylthio, C₁-C₄alkylsulfinyl, C₁-C₄ alkylsulfonyl, C₁-C₄ alkylamino, C₂-C₈dialkylamino, C₃-C₆ cycloalkylamino, C₃-C₆ (alkyl)cycloalkylamino, C₂-C₄alkylcarbonyl, C₂-C₆ alkoxycarbonyl, C₂-C₆ alkylaminocarbonyl, C₃-C₈dialkylaminocarbonyl or C₃-C₆ trialkylsilyl.
 30. The compound of claim29 wherein J is selected from the group consisting of pyridine,pyrimidine, pyrazole, imidazole, triazole, thiophene, thiazole andoxazole, furan, isothiazole and isoxazole, each optionally substitutedwith 1 to 3 R⁷.
 31. The compound of claim 30 wherein J is selected fromthe group consisting of pyridine, pyrimidine, pyrazole, thiophene andthiazole, each optionally substituted with 1 to 3 R⁷; R¹ and R² are bothH; R³ is C₁-C₄ alkyl optionally substituted with halogen, CN, OCH₃,S(O)_(p)CH₃; each R⁴ is independently H, CH₃, CF₃, OCF₃, OCHF₂,S(O)_(p)CF₃, S(O)_(p)CHF₂, CN or halogen; each R⁷ is independently H,halogen, CH₃, CF₃, OCHF₂, S(O)_(p)CF₃, S(O)_(p)CHF₂, OCH₂CF₃, OCF₂CHF₂,S(O)_(p)CH₂CF₃, S(O)_(p)CF₂CHF₂; or phenyl, pyrazole, imidazole,triazole, pyridine or pyrimidine, each ring optionally substituted withC₁-C₄ alkyl, C₁-C₄ haloalkyl, C₁-C₄ alkoxy, C₁-C₄ haloalkoxy, C₁-C₄alkylthio, C₁-C₄ alkylsulfinyl, C₁-C₄ alkylsulfonyl, halogen or CN; andp is 0, 1 or
 2. 32. The compound of claim 31 wherein J is a pyridineoptionally substituted with 1 to 3R⁷.
 33. The compound of claim 32wherein one R⁷ is a phenyl optionally substituted with C₁-C₄ alkyl,C₁-C₄ haloalkyl, halogen or CN.
 34. The compound of claim 32 wherein oneR⁷ is a pyrazole, imidazole, triazole, pyridine or pyrimidine, each ringoptionally substituted with C₁-C₄ alkyl, C₁-C₄ haloalkyl, halogen or CN.35. The compound of claim 31 wherein J is a pyrimidine optionallysubstituted with 1 to 3 R⁷.
 36. The compound of claim 35 wherein one R⁷is a phenyl optionally substituted with C₁-C₄ alkyl, C₁-C₄ haloalkyl,halogen or CN.
 37. The compound of claim 35 wherein one R⁷ is apyrazole, imidazole, triazole, pyridine or pyrimidine, each ringoptionally substituted with C₁-C₄ alkyl, C₁-C₄ haloalkyl, halogen or CN.38. The compound of claim 32 wherein J is a pyrazole optionallysubstituted with 1 to 3 R⁷.
 39. The compound of claim 38 wherein one R⁷is a phenyl optionally substituted with C₁-C₄ alkyl, C₁-C₄ haloalkyl,halogen or CN.
 40. The compound of claim 38 wherein one R⁷ is apyrazole, imidazole, triazole, pyridine or pyrimidine, each ringoptionally substituted with C₁-C₄ alkyl, C₁-C₄ haloalknyl, halogen orCN.
 41. The compound of claim 38 wherein wherein R⁷ is a pyridineoptionally substituted with C₁-C₄ alkyl, C₁-C₄ haloalkyl, halogen or CN.42. The compound of claim 22 selected from the group consisting of:3-methyl-N-(1-methylethyl)-2-[[4-(trifluoromethyl)benzoyl]amino]-benzamide,2-methyl-N-[2-methyl-6-[[(1-methylethyl)amino]carbonyl]phenyl]-4-(trifluoromethyl)benzamide,2-methyl-N-[2-methyl-6-[[(1-methylethyl)amino]carbonyl]phenyl]-6-(trifluoromethyl)-3-pyridinecarboxamide,1-ethyl-N-[2-methyl-6-[[(1-methylethyl)amino]carbonyl]phenyl]-3-(trifluoromethyl)-1H-pyrazole-5-carboxamide,1-(2-fluorophenyl)-N-[2-methyl-6-[[(1-methylethyl)amino)carbonyl]phenyl]-3-(trifluoromethyl)-1H-pyrazole-5-carboxamide,b1-(3-chloro-2-pyridinyl)-N-[2-methyl-6-[[(1-methylethyl)amino]carbonyl]phenyl]3-(trifluoromethyl)-1H-pyrazole-5-carboxamide,N-[2-chloro-6-[[(1-methylethyl)amino]carbonyl]phenyl]-1-(3-chloro-2-pyridinyl)-3-(trifluoromethyl)-1H-pyrazole-5-carboxamide,3-bromo-1-(2-chlorophenyl)-N-[2-methyl-6-[[(1-methylethyl)amino]carbonyl]phenyl]-1H-pyrazole-5-carboxamide,and3-bromo-N-[2-chloro-6-[[(1-methylethyl)amino]carbonyl]phenyl]-1-(2-chlorophenyl)-1H-pyrazole-5-carboxamide.43. An arthropodicidal composition comprising an arthropodicidallyeffective amount of a compound of Formula 1 as described in claim 1 andat least one additional component selected from the group consisting ofsurfactants, solid diluents and liquid diluents.